The Recall Desk

Archive

March 2025 recalls

446 recalls were announced in March 2025.

What the numbers show

Critical
7
Severe
95
High
303
Moderate
37
Low
4

Of the 446 recalls this month scored against our rubric, 2% are Critical, 21% are Severe.

Which agencies issued them

101–200 of 446

  • HighFDA (Devices)·Z-1381-2025·2025-03-26

    Microstream CO2 Intubated Filter Lines Difficult to Disconnect

    Microstream CO2 filter lines used with intubated patients may be difficult or impossible to disconnect from the endotracheal tube, potentially delaying treatment or causing unintended extubation.

    Product
    Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv. Adult-Pediatric Intubated, PT00134333 - Microstream Advance Adult-Pediatric Intubated CO2 Filter Line 2m/6.5ft Short-term use: Procedural/Emergency, QMVAI…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0283-2025·2025-03-26

    Walgreens Acne Cream Recalled for Benzene Contamination

    Walgreens Maximum Strength Tinted Acne Treatment Cream is being recalled for benzene contamination. The product was distributed nationwide; affected consumers should stop use immediately.

    Product
    Walgreens Maximum Strength Tinted Acne Treatment Cream 10% Benzoyl Peroxide/Acne Medication, 0.65 oz (18.4g) tube in a carton; Distributed by: Walgreen CO., 200 Wilmot Rd., Deerfield, IL 60015
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1362-2025·2025-03-26

    Vein Tray Models UTVT21C Unable to Confirm Sterilization Assurance

    American Contract Systems Inc is recalling certain Vein Tray models because sterilization assurance requirements could not be confirmed. The affected units may lack functionality and could lead to delayed treatment.

    Product
    VEIN TRAY, Model No UTVT21C UTVT21C02 UTVT21C-03
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1349-2025·2025-03-26

    Laceration Trays Recalled Due to Sterility Assurance Concerns

    American Contract Systems Inc recalled 690 laceration trays because the company cannot confirm sterilization assurance requirements were met. The recalled devices may lose functionality, potentially delaying or prolonging patient treatment.

    Product
    LACERATION TRAY , Model No SGLA07A SGLA07B-01 SGLA07B-02 SGLA07B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0640-2025·2025-03-26

    Madras Curry Powder Recalled for Elevated Lead Levels

    Trong Food International is recalling Madras Curry Powder sold in three package sizes due to elevated lead contamination. All lots of the product have been included in the recall, which affected distributors in Maryland and Washington DC.

    Product
    Madras Curry Powder sold in 3 different package sizes. Recall has been expanded to include ALL LOTS. CA RI NI AN DO "KIM TU THAP", NET WT./ Poids NET (4oz.) 114 grams glass jar UPC# 39606001562 (4oz.) 114 grams plastic pouch UPC# 36906001544 (16oz.) plastic bottle UPC#…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1375-2025·2025-03-26

    BD Pyxis Medication Dispensing Systems Software Sync Error Recall

    BD Pyxis medication dispensing systems may disconnect from their server due to a software error, preventing them from receiving medication updates. This could lead to incorrect medication administration or delayed access to medications.

    Product
    BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF: 1116-00, CII Safe ES Desktop PC, REF: 1156-00, CII Safe ES Desktop PC, Wired SCNR, REF: 107-254-01, CII Safe ES Desktop PC, W-less SCNR, REF: 107-255-01…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1359-2025·2025-03-26

    Cardiac Surgical Training Kits Recalled for Sterilization Verification Failure

    American Contract Systems Inc is recalling OPEN HEART A PACK surgical training kits (Models UTOH19AI, UTOH19AJ-01, UTOH19AJ-02) because sterilization assurance requirements cannot be confirmed. Lack of sterilization could impair functionality.

    Product
    OPEN HEART A PACK , Model No UTOH19AI UTOH19AJ-01 UTOH19AJ-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1379-2025·2025-03-26

    CO2 Sampling and Airway Adapter Devices May Be Difficult to Disconnect

    Oridion Medical's CO2 sampling and airway adapter devices may be difficult to disconnect from endotracheal tubes, potentially causing treatment delays and serious respiratory complications in neonatal, infant, and pediatric patients.

    Product
    Microstream Instructions for Use and Part Number used with - Product Description, REF: Airway Adapter and CO2 Sampling Line, 01158 - Microstream Luer Adult-Pediatric Airway Adapter, 010989; Omnistream CO2 Sampling Line X25, 010991
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1344-2025·2025-03-26

    Labor and Delivery System Recalled for Sterilization Assurance Issue

    American Contract Systems is recalling 1,836 Labor and Delivery PPS kits due to inability to confirm sterilization requirements were met. The affected units may lose functionality, potentially delaying patient treatment.

    Product
    LABOR & DELIVERY PPS , Model No LLLD64O LLLD64O-01 LLLD64O-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1402-2025·2025-03-26

    Merge Cardio Software Recalled: Measurement Inconsistency in Patient Reports

    Merge Healthcare recalls Merge Cardio cardiovascular software due to measurement data inconsistency. When users manually edit or remeasure values in certain workflows, derived measurements may not match original measurements in patient reports.

    Product
    Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.1, 12.1.1, 12.2, 12.3, 12.3.1, 12.3.2, 12.3.3, 12.4, 12.4.1, 12.4.2; Merge Cardio is a software medical device that is an integrated multi-modality image cardiovascular information management system.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1407-2025·2025-03-26

    Synapse PACS Software incorrect patient age calculation for infants

    FUJIFILM's Synapse PACS Software versions 7.4.x incorrectly calculates patient age for infants under 3 months, potentially affecting clinical decisions. 104 units recalled in US and internationally.

    Product
    Synapse PACS Software Version 7.4.x; Software Versions: 7.4.000, 7.4.001, 7.4.010, 7.4.100, 7.4.110, 7.4.200.
    Category
    Medical Device
    Distribution
    30 states
  • HighFDA (Drugs)·D-0279-2025·2025-03-26

    Cinacalcet Hydrochloride Tablets Recalled for Nitrosamine Impurity Above Safe Limits

    Slate Run Pharmaceuticals is recalling Cinacalcet Hydrochloride Tablets 60 mg for containing nitrosamine impurity above acceptable daily intake limits. The recall affects 2,444 bottles distributed nationwide.

    Product
    Cinacalcet Hydrochloride Tablets 60 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-008-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1384-2025·2025-03-26

    Microstream CO2 Sampling Line Disconnection Failure Poses Respiratory Risk

    Microstream CO2 sampling adapters may become difficult or impossible to disconnect from endotracheal tubes, potentially delaying critical procedures and causing respiratory complications.

    Product
    Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Advance Intubated Adult-Pediatric, PT00156254 - Microstream Advance Adult-Pediatric Intubated CO2 Filter Line 2m/6.5ft Short-term use: Procedural/Emergency, MVAI…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1395-2025·2025-03-26

    Zebra Thermal Barcode Printer power supply units recalled due to fire hazard

    Remel, Inc. is recalling approximately 41 Zebra Thermal Barcode Printer GX430t power supply units due to a potential fire hazard. The power supplies may overheat, creating a fire risk.

    Product
    Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an optional accessory for Sensititre Aris HIQ system YV4000-VZ
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Devices)·Z-1334-2025·2025-03-26

    Medical Device Sterilization Assurance Recall: MAJOR DIEP Surgical Kits

    American Contract Systems Inc is recalling 17 MAJOR DIEP surgical kits because sterilization assurance requirements cannot be confirmed. This creates a risk of device malfunction and treatment delays.

    Product
    MAJOR DIEP, Model Nos. CCMJ73G-01 CCMJ73H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0278-2025·2025-03-26

    Cinacalcet Hydrochloride Tablets Recalled for Nitrosamine Impurity

    Slate Run Pharmaceuticals is recalling Cinacalcet Hydrochloride Tablets 30 mg due to nitrosamine impurity above acceptable daily intake limits. 56,790 bottles were distributed to 8 wholesalers nationwide.

    Product
    Cinacalcet Hydrochloride Tablets 30 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-007-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1341-2025·2025-03-26

    Birth Delivery Kit Recalled Due to Unconfirmed Sterilization Assurance

    American Contract Systems Inc recalls the Born on Arrival Kit due to inability to confirm sterilization assurance. Unsterilized equipment could delay or prolong newborn treatment.

    Product
    BORN ON ARRIVAL KIT , Model No LLBN11B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1335-2025·2025-03-26

    Cystoscopy Kit Recalled for Sterilization Assurance Verification Failure

    American Contract Systems Inc is recalling CYSTO PACK cystoscopy kits because the company cannot confirm sterilization assurance requirements were met. Possible loss of functionality could delay or prolong patient treatment.

    Product
    CYSTO PACK , Model N. HKCY31A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1331-2025·2025-03-26

    Laparoscopy Surgical Packs Recalled Due to Unconfirmed Sterilization

    American Contract Systems Inc. is recalling 303 Laparoscopy Packs (Models CALS41F, CALS41F-01, CALS41G) because sterilization assurance requirements could not be confirmed. Unsterilized instruments may cause infection or delayed treatment.

    Product
    LAPAROSCOPY PACK, Model No. CALS41F, CALS41F-01, CALS41G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1364-2025·2025-03-26

    Surgical Drape Packs Recalled for Potential Sterility Breach in Packaging

    Medline Industries is recalling Proxima Sterile Surgical Drape packs due to a potential breach in the pouch packaging that could lead to loss of sterility. The recall affects 1,490 units distributed nationwide.

    Product
    Proxima Drape labeled as PACK,BASIC,SIRUS,V,5/CS; PACK,BASIC IV,SIRUS,5/CS; PACK,SET UP,NO DRAPE,12/CS; PACK,SET UP,NO DRAPE,12/CS; PACK,SET UP,NO DRAPE,12/CS; PACK,SET UP,NO DRAPE,12/CS; PACK,SET UP,NO DRAPE,12/CS; PACK,UNIVERSAL II,SIRUS,7/CS; PACK,LAPAROTOMY,NO GOWN,10/CS…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0289-2025·2025-03-26

    FDA Recalls Subpotent CURAD Alcohol Prep Pads Nationwide

    Medline Industries is recalling CURAD Alcohol Prep Pads nationwide because they are subpotent. The recalled pads are sterile, medium, 2-ply alcohol prep pads distributed nationally.

    Product
    CURAD ALCOHOL PREP PADS — CURAD ALCOHOL PREP PADS (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1400-2025·2025-03-26

    VERICIS Merge Cardio Medical Device Software Measurement Data Consistency Issue

    VERICIS Merge Cardio cardiovascular imaging software may display measurement values in patient reports that do not match original measurements when measurements are remeasured or manually edited. This affects 66 units distributed in the United States.

    Product
    VERICIS, Merge Cardio, Model/Catalog Number: Version 11.x, Software Version: 11.0.2, 11.0.3, 11.0.4, 11.1, 11.1.1; The VERICIS is an integrated cardiovascular information system classified as a picture archiving and communications system.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1380-2025·2025-03-26

    CO2 Sampling Line Adapter May Be Difficult to Disconnect; Risk of Respiratory Failure

    Microstream CO2 sampling line and airway adapter may be difficult or impossible to disconnect during procedures, potentially causing treatment delays and respiratory complications including hypoxia.

    Product
    Microstream Instructions for Use and Part Number used with - Product Description, REF: OmniVentLine Set, 012808 - OmniVentLine Set Adult-Pediatric CO2 Sampling Line and Airway Adapter, 012495;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0291-2025·2025-03-26

    FDA Recalls Super-Potent Levothyroxine Sodium Tablets Due to Potency Deviation

    Mylan Institutional is recalling 1,068 cartons of levothyroxine sodium 125 mcg tablets (Lot 3115773) distributed nationwide due to out-of-specification potency. The tablets contain higher-than-specified amounts, potentially resulting in excessive doses.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1346-2025·2025-03-26

    CYSTO Model SACY80R Recall for Sterilization Assurance Failure

    American Contract Systems Inc is recalling 144 CYSTO Model SACY80R kits due to inability to confirm sterilization requirements were met. Unsterilized devices may lose functionality and delay patient treatment.

    Product
    CYSTO , Model No SACY80R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1404-2025·2025-03-26

    CAPNOCHECK BCI Airway Adapter may break off, causing ventilation failure

    The CAPNOCHECK BCI Airway Adapter (Model BSR) may break when attached to a valve or tube, risking airway circuit failure and loss of ventilation. Approximately 175,994 units were recalled nationwide.

    Product
    CAPNOCHECK BCI Airway Adapter; Model Number BSR; Product Code WW1100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1355-2025·2025-03-26

    Neuro IR Tray recalled over unconfirmed sterilization assurance

    American Contract Systems Inc is recalling Neuro IR Tray (Model WENI56J) due to inability to confirm sterilization assurance. Loss of functionality could delay or prolong treatment.

    Product
    NEURO IR TRAY , Model No WENI56J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1332-2025·2025-03-26

    DR DIULUS Injection Pack Models Recalled for Sterilization Assurance Issues

    American Contract Systems Inc is recalling 1,200 DR DIULUS Injection Pack kits because the manufacturer cannot confirm sterilization assurance requirements were met. This may result in loss of functionality and treatment delays.

    Product
    DR DIULUS INJECTION PACK, Model Nos. CCDU12C CCDU12D CCDU12D-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1383-2025·2025-03-26

    Microstream CO2 Sampling Line May Not Disconnect From Intubation Tube

    Microstream intubated CO2 sampling lines may be difficult or impossible to disconnect from endotracheal tubes. This could delay necessary procedures and cause unintended extubation, potentially leading to respiratory failure.

    Product
    Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Luer Intubated Adult Pediatric, PT00156355 - Microstream Luer Adult-Pediatric Intubated CO2 Sampling Line 2m/6.5ft Short-term use: Procedural/Emergency, MLAI
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1339-2025·2025-03-26

    Open Heart Surgery Kit Sterilization Assurance Cannot Be Confirmed

    American Contract Systems Inc is recalling 90 Open Heart Adult Side A surgical kits due to inability to confirm sterilization requirements were met. Unsterilized devices could lose functionality and delay patient treatment.

    Product
    OPEN HEART ADULT - SIDE A , Model Nos LLOH01I-01 LLOH01I
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0648-2025·2025-03-26

    Dried Longan Pulp Recalled for Elevated Sulfite Levels

    Growland Inc. is recalling Dried Longan Pulp products due to elevated sulfite levels. The affected product was distributed across seven states.

    Product
    Dried Longan Pulp- Made in China, 8oz(227g), GROWLAND INC. rear panel- Organic Planted, Store in cool and dry place, Made in Thailand; UPC# 8 513041 327262
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0639-2025·2025-03-26

    Domna's Bakery Baklava Recalled for Undeclared Milk Allergen

    Optima Foods is recalling Domna's Bakery 24 PC Baklava Tray distributed in New York because it contains undeclared milk. Consumers with milk allergies should not consume this product.

    Product
    Domna's Bakery 24 PC Baklava Tray 330043 8
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1382-2025·2025-03-26

    Microstream Neonatal-Infant CO2 Filter Line May Be Difficult to Disconnect

    Microstream Neonatal-Infant Intubated CO2 Filter Lines may become difficult or impossible to disconnect from endotracheal tubes during clinical procedures, potentially delaying treatment and causing unintended extubation.

    Product
    Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstream Adv. Infant Intubated, PT00134354 - Microstream Advance Neonatal-Infant Intubated CO2 Filter Line 2m/6.5ft Extended Duration, QMVIIH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1405-2025·2025-03-26

    CAPNOCHECK Airway Adapter May Break Off, Risking Ventilation Loss

    CAPNOCHECK BCI Airway Adapters may break off when a valve or tube is attached, causing airway circuit disconnection and loss of ventilation. This could result in inability to ventilate, hypoxia, cardiopulmonary collapse, or death.

    Product
    CAPNOCHECK BCI Airway Adapter; Model Number BSR; Product Code WW8214
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0641-2025·2025-03-26

    Shredded Colby Jack cheese recalled for potential stainless steel fragments

    Great Lakes Cheese Co is recalling Happy Farms by ALDI Colby Jack shredded cheese due to potential stainless steel fragments. Affected products have best-by dates of July 13 or July 14, 2025.

    Product
    Happy Farms by ALDI Colby Jack (a blend of Colby & Monterey Jack finely shredded cheeses), Net Wt. 12 OZ (340g), packaged in flexible plastic stand-up pouches, 12 pouches per case, UPC 4061463330840, with Best By dates of July 13, 2025 and July 14, 2025. Dist. & sold exclusively…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1358-2025·2025-03-26

    Vascular Pack Sterilization Assurance Requirements Cannot Be Confirmed

    American Contract Systems cannot confirm Major Vascular Pack surgical kits were properly sterilized. Sterilization assurance failure could result in loss of functionality and delayed patient treatment.

    Product
    MAJOR VASCULAR PACK , Model No UTMV78X-01 UTMV78Y UTMV78Y-01 UTMV78X-01 UTMV78Y-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1406-2025·2025-03-26

    Cranial Surgery Procedure Kit Recalled Over Sterility Assurance Failure

    American Contract Systems Inc is recalling 91 CRANI PACK cranial procedure kits because a critical component cannot be confirmed to meet sterility requirements, making them unsuitable for surgical use.

    Product
    CRANI PACK, Model/Catalog Number WECR41D, medical procedure kit.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1372-2025·2025-03-26

    Modular Stem Orthopedic Implant Recalled Due to Incorrect Product Identifier

    37 units of a modular stem orthopedic implant (Product Code 880-601/11) have been recalled due to an incorrect GTIN product identifier on the carton label, which belongs to a different product. No illnesses or injuries have been reported.

    Product
    Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm, DIA = 11 mm, Product Code: 880-601/11
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1386-2025·2025-03-26

    Access 2 Immunoassay Analyzer motor alignment issue may delay results

    Beckman Coulter is recalling Access 2 Immunoassay Analyzers due to sample motor misalignment that may delay patient test result reporting. The recall affects 873 units distributed worldwide.

    Product
    Access 2 Immunoassay Analyzer, Catalog Number 81600N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1374-2025·2025-03-26

    Modular Stem Orthopedic Implants Recalled for Incorrect GTIN Labeling

    Waldemar Link is recalling 20 units of Modular Stem orthopedic implants due to incorrect GTIN labeling on the outer carton. The label bears a barcode for a different product.

    Product
    Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm, DIA = 13 mm, Product Code: 880-601/13
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0288-2025·2025-03-26

    Medline Alcohol Prep Pads Recalled for Subpotent Isopropyl Alcohol

    Medline Industries has voluntarily recalled over 6.6 million alcohol prep pads nationwide because the product contains less isopropyl alcohol than labeled. The subpotent product was first reported on March 26, 2025.

    Product
    MEDLINE ALCOHOL PREP — MEDLINE ALCOHOL PREP (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0282-2025·2025-03-26

    Ciprofloxacin Ophthalmic Solution Recalled Nationwide for Defective Container Cap

    Ciprofloxacin Ophthalmic Solution is being recalled because the cap spike is lodged in the bottle nozzle, preventing patients from accessing the medication. Affected lot 084A067 was distributed nationwide.

    Product
    CIPROFLOXACIN — CIPROFLOXACIN (CIPROFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1373-2025·2025-03-26

    Hip Prosthetic Stem Recalled for Incorrect Product Code Label

    A modular hip prosthetic stem (52 units) is being recalled due to an incorrect GTIN barcode on the outer carton label, which displays the code for a different product. No injuries have been reported.

    Product
    Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm, DIA = 12 mm, Product Code: 880-601/12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1387-2025·2025-03-26

    Beckman Coulter DxI 9000 Analyzer Communication Failure Recall

    Beckman Coulter recalls certain DxI 9000 immunoassay analyzers due to firmware issues that can cause communication failures, potentially delaying patient result reporting.

    Product
    DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, with Component PCB, TSI/RSI firmware C29278
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1371-2025·2025-03-26

    Helix Elite SARS-CoV-2 QC Material Recall Due to Potential Ct Value Issues

    Microbiologics Inc is recalling Helix Elite Inactivated SARS-CoV-2 quality control material (Lot HE0065-29) because the A549 human cell target may produce late Ct values, potentially affecting test result validity.

    Product
    Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus (Pellet), Multi-analyte, unassayed quality control material, Catalog Number HE0065N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1391-2025·2025-03-26

    IsoLoc Prostate Treatment Balloon Devices Recalled for Incorrect Fill Volume Labeling

    Angiodynamics is recalling 1,800 units of IsoLoc prostate treatment balloons due to incorrect fill volume labeling. The affected devices were distributed nationwide.

    Product
    IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit; UPN/Catalog Number: ISO-60;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V055000·2025-03-25

    Volvo Recalls 2023-2025 VNR Electric Trucks Due to Battery Fire Risk

    Volvo Trucks North America is recalling 2023-2025 VNR Electric trucks because loose hardware in the high-voltage battery may cause a short circuit and fire.

    Product
    VOLVO — VOLVO VNRE (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V183000·2025-03-25

    Keystone travel trailer patio latch screws can loosen during transit

    Keystone RV is recalling certain 2025 Kodiak 2900FKSP and 308BHSL travel trailers because the patio latch screws may loosen, causing the latch to detach during transit.

    Product
    KEYSTONE — KEYSTONE KODIAK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V187000·2025-03-25

    2025–2026 Western Star and Freightliner trucks recalled for brake light failure

    Daimler Trucks North America is recalling certain 2025–2026 Western Star 47X and 49X and multiple Freightliner models due to a software error that may cause brake lights to fail, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR BUSINESS CLASS M2, 47X, 49X, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V181000·2025-03-24

    Peterbilt and Kenworth high voltage contactors can open cutting drive power

    PACCAR is recalling certain 2021-2025 Peterbilt 520, 579 and Kenworth T680 trucks because the high voltage contactors may open, causing a sudden loss of high voltage and drive power.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, 579, 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V179000·2025-03-24

    Volvo Recalls Plug-In Hybrids Due to High-Voltage Battery Fire Risk

    Volvo is recalling specific 2020-2022 plug-in hybrid models because a high-voltage battery short circuit could cause a fire. Owners should stop charging until repairs are completed.

    Product
    VOLVO — VOLVO S90, XC60, V60, S60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V182000·2025-03-24

    PACCAR Recalls Kenworth and Peterbilt Electric Trucks for Electrical Defect

    PACCAR is recalling specific Kenworth and Peterbilt electric trucks because a loose electrical connection in the cradle harness may cause a loss of drive power, increasing crash risk.

    Product
    KENWORTH — KENWORTH, PETERBILT K270, K370, 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V178000·2025-03-21

    International truck calipers can contact suspension stopping the outer brake pad

    International is recalling certain 2019-2025 HV, MV and Workstar 7400 trucks because the caliper may contact a suspension spring or axle U-bolt and prevent the outer brake pad functioning.

    Product
    INTERNATIONAL — INTERNATIONAL MV, HV, WORKSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25187·2025-03-20

    Aiper Seagull Pro Cordless Pool Cleaners Recalled for Fire and Burn Hazards

    About 32,660 Aiper Seagull Pro pool cleaners are recalled because the power adapter can overheat and catch fire. The firm reported 19 incidents of melting, smoking or fires, resulting in 5 property damage claims with no injuries.

    Product
    Aiper Seagull Pro ZT6001 cordless robotic pool cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25193·2025-03-20

    Segway Ninebot Max G30P and G30LP KickScooters Recalled for Fall Hazard

    The folding mechanism on about 220,000 Segway Ninebot Max G30P and G30LP KickScooters can fail during use, causing the handlebars to fold and posing a fall hazard. Segway has received 68 reports of failures, including 20 injuries.

    Product
    Segway Ninebot Max G30P and Max G30LP KickScooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25188·2025-03-20

    Model Year 2025 Ski-Doo and Lynx Snowmobiles Recalled for Engine Mount Failure

    Bombardier Recreational Products recalls about 4,144 Model Year 2025 Ski-Doo and Lynx snowmobiles due to engine control module mounts that may break and cause stuck throttle, creating a crash hazard.

    Product
    Model Year 2025 Ski-Doo and Lynx snowmobiles equipped with a 600R E-TEC, 850 E-TEC or 850 E-TEC Turbo R engine
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25191·2025-03-20

    Bella Pro Series and Cooks espresso machines recalled due to burn and laceration hazards

    Sensio recalls about 12,300 Bella Pro Series and Cooks Steam Espresso machines because the brew cup handle can eject forcefully, shattering the carafe. Eight of 18 ejection reports involved burn and laceration injuries.

    Product
    Bella Pro Series and Cooks Steam Espresso machines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·008-2025·2025-03-20

    Idaho Smokehouse Recalls Beef Sticks Due to Possible Metal Contamination

    Idaho Smokehouse Partners is recalling approximately 29,541 pounds of Chomps Original Beef Stick Mild products due to possible metal contamination. Consumers are advised not to consume the affected items.

    Product
    Idaho Smokehouse Partners LLC — Idaho Smokehouse Partners Recalls Ready-To-Eat Beef Stick Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·25189·2025-03-20

    Woolite Delicates Detergent Recalled Due to Bacterial Contamination Risk

    Reckitt is recalling approximately 16,200 bottles of Woolite Delicates detergent sold exclusively on Amazon due to potential Pseudomonas bacteria contamination. The bacteria poses a serious infection risk to people with weakened immune systems or external medical devices.

    Product
    Woolite Delicates detergent in 50-fluid-ounce bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25190·2025-03-20

    Wireless portable power banks recalled due to fire and burn hazards

    VC Group recalls 89,500 MagSafe wireless power banks because lithium-ion batteries can overheat and ignite. The company received 19 fire reports resulting in 10 minor injuries.

    Product
    VC Group MagSafe Wireless Power Pack Portable Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V174000·2025-03-20

    Jeep Wagoneer S headlights cannot be aimed properly

    Chrysler is recalling certain 2024-2025 Jeep Wagoneer S electric vehicles because the headlight vertical aim adjustment is not accessible and the horizontal aim is not covered, failing FMVSS 108.

    Product
    JEEP — JEEP WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25194·2025-03-20

    Benadryl Liquid Elixir 100 mL bottles lack child-resistant packaging

    Arsell is recalling Benadryl Liquid Elixir 100 mL bottles sold on Amazon because the packaging is not child-resistant as required by federal law. The medication could poison children if ingested.

    Product
    Benadryl Liquid Elixir, 100 mL bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·25V175000·2025-03-20

    GM Recalls 2016-2018 Cadillac and Chevrolet Vehicles for Steering Defect

    General Motors is recalling specific 2016-2018 Cadillac and Chevrolet vehicles because the electric power steering assist may fail, increasing crash risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET CTS, CAMARO, ATS, CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V171000·2025-03-20

    Thor Motor Coach motorhomes slide-out room unexpected deployment risk

    Thor Motor Coach is recalling certain 2023–2026 motorhomes because the slide-out room can extend while the vehicle is moving, increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FREEDOM TRAVELER, FREEDOM ELITE, AXIS, VEGAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V176000·2025-03-20

    IC school bus low beams turn off with high beams

    International is recalling certain 2025-2026 IC Bus CESB school buses with halogen headlights because activating the high beams turns the low beams off, failing FMVSS 108.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25192·2025-03-20

    GIKPAL 10 Drawer Dressers Recalled for Tip-Over and Entrapment Risk to Children

    GIKPAL 10 Drawer Dressers sold on Walmart.com are recalled for tip-over and entrapment hazards to children if not anchored to a wall. About 28,590 units were sold between September 2023 and January 2025.

    Product
    GIKPAL 10 Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25184·2025-03-20

    Adjustable Dumbbells Recalled for Weight Plate Dislodging Impact Hazard

    Weight plates on FitRx SmartBell XL dumbbells can dislodge during use, causing impact injuries. More than 60 incidents reported, linked to 7 documented injuries including bruises and contusions.

    Product
    FitRx SmartBell XL Quick-Select 10-90 lbs. Adjustable Dumbbells
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0633-2025·2025-03-19

    Ulker Biskrem Cocoa Biscuits Recalled for Undeclared Wheat and Egg

    ZB Importing LLC recalls Ulker Biskrem Cocoa Biscuits due to undeclared wheat and egg. Consumers with these allergies should not consume the product.

    Product
    Ulker Biskrem Cocoa Biscuit, item 8836, 10.6oz foil pack, 8 per case, UPC 8690504114628
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Devices)·Z-1289-2025·2025-03-19

    Portex Endotracheal Tubes may deliver inadequate ventilation due to smaller diameter

    Portex Endotracheal Tubes from Smiths Medical ASD, Inc. may have a smaller diameter than expected, potentially causing inadequate ventilation and patient hypoxia.

    Product
    Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035 100/111/035 100/126/025 100/126/030 100/126/035 100/127/025 100/127/030 100/127/035 100/141/025 100/141/030 100/141/035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0609-2025·2025-03-19

    Aleppo Tahini Sesame Paste recalled due to Salmonella contamination

    Turkana Food Inc. is recalling Aleppo Tahini Sesame Paste because the product tested positive for Salmonella. The recalled product was distributed to 23 states.

    Product
    Aleppo Tahini Sesame Paste, 32oz, Plastic jar, 1lb (16oz), 12 per case
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Food)·F-0636-2025·2025-03-19

    Mauna Loa Milk Chocolate Macadamias recalled for undeclared almonds

    Mauna Loa Macadamia Nut Company is recalling Milk Chocolate Covered Macadamias due to undeclared almonds. The product may cause allergic reactions in consumers with almond or tree nut allergies.

    Product
    Mauna Loa Milk Chocolate Covered Macadamias product is a snack product and packaged in plastic 1oz pouch. Each carton contains 12 pouches, and each master case contains 12 cartons. Retail Pouch (1oz pouch) UPC: 0 72992 04260 3 Carton (12 pouches) UPC: 72992 04261 Master Case…
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0268-2025·2025-03-19

    Potassium Chloride Injection Strength Mislabeled on Packaging Overwrap

    ICU Medical recalls Potassium Chloride Injection (lot 1023172) whose overwrap labeled as 10 mEq may contain 20 mEq containers, creating overdose risk. Product distributed nationwide.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0259-2025·2025-03-19

    ChloraPrep One-Step Topical Drug Recalled for Fungal Contamination

    CareFusion 213, LLC is recalling ChloraPrep One-Step, a preoperative skin preparation drug, due to non-sterility from a package lidding breach allowing fungal contamination. The recall affects 205,440 applicators distributed nationwide and in Canada.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0608-2025·2025-03-19

    Raisin Bran Muffins Recalled Due to Undeclared Walnut Allergen

    JE Bakery 2019 LLC is recalling Raisin Bran muffins sold under Cub Foods, Jerrys Foods, and County Market brands due to undeclared walnuts. The product was distributed in Minnesota and Wisconsin.

    Product
    Raisin Bran muffins, 6 count. Net Wt. 12.0 oz (0.75 lb) UPC 0 29341-00233 7. Labeled with the following store brands: Cub Foods, Jerrys Foods, and County Market
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1304-2025·2025-03-19

    BD Alaris Systems Manager Infusion Software Affected by Programming Request Issue

    BD Alaris Systems Manager software may transmit outdated automated programming requests to progressive care units. The FDA has classified this as a Class I recall.

    Product
    BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
    Category
    Medical Device
    Distribution
    21 states
  • SevereFDA (Food)·F-0637-2025·2025-03-19

    Little Leaf Farms Southwest Salad Kit Recalled for Undeclared Fish and Wheat

    Little Leaf Farms Southwest Salad Kit may contain incorrect dressing with undeclared fish and wheat. The recalled lot was distributed in Massachusetts, New Hampshire, and Connecticut.

    Product
    Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UPC: 857394006220
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1305-2025·2025-03-19

    BD Care Coordination Engine Software May Send Outdated Programming Requests

    BD Care Coordination Engine infusion software may send outdated automated programming requests to care units. Healthcare facilities in affected US states should review their systems.

    Product
    BD Care Coordination Engine (CCE) Infusion Adapter, Safety Management Software
    Category
    Medical Device
    Distribution
    21 states
  • SevereFDA (Devices)·Z-1306-2025·2025-03-19

    Aortic Root Cannula Recall for Loose Male Luer Component

    Medtronic is recalling 316,205 aortic root cannulas due to unexpected loose material in the male luer connector. If not identified before use, this defect could cause stroke; if identified, it may delay surgery.

    Product
    Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, model no 11012 B. CANNULA 11014 AR FLOWGUARD 14GA, model no. 11014 2. MiAR Cannula: A. CANNULA 11012L AR FLOWGUARD LONG 12GA, model no 11012L B. CANNULA 11014L AR FLOWGUARD 14FR LONG…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0267-2025·2025-03-19

    Potassium Chloride Injection Recalled: Overwrap Labeling Shows Incorrect Strength

    ICU Medical recalls Potassium Chloride 20 mEq IV injection due to mislabeled overwrap showing 10 mEq instead of the correct strength. The correct dose is printed on the actual container.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0272-2025·2025-03-19

    Injectable Phenylephrine Solution Recalled Due to Particulate Matter Contamination

    The FDA is recalling phenylephrine injection solution due to particulate matter contamination. Three lot numbers distributed nationwide are affected.

    Product
    PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), Rx Only, CAPS, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, 855-275-2270, NDC 71285-6092-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V173000·2025-03-19

    Nissan and INFINITI front brake calipers may break losing braking

    Nissan is recalling certain 2025 Murano, Pathfinder and INFINITI QX60 vehicles because one or both front brake caliper assemblies may have reduced strength and could break, failing FMVSS 135.

    Product
    INFINITI — INFINITI, NISSAN QX60, PATHFINDER, MURANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E020000·2025-03-19

    ZF Recalls Lemförder and TRW Track Control Arms for Subframe Cracking Risk

    ZF North America is recalling specific Lemförder and TRW track control arms because a short bushing sleeve may crack the subframe, potentially causing loss of vehicle control.

    Product
    SUSPENSION:FRONT:CONTROL ARM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0631-2025·2025-03-19

    Ulker Rulokat hazelnut wafers recalled nationwide for undeclared egg allergen

    Ulker Rulokat Hazelnut Wafers are being recalled due to undeclared egg. The product was distributed to retail stores across Canada and 35 US states.

    Product
    Ulker Rulokat Hazelnut Wafers, item 3865, 6oz plastic cylinder, 6 per case, UPC 8690766086473
    Category
    Food
    Distribution
    36 states
  • HighNHTSA·25V172000·2025-03-19

    Tesla Model S and X may have an inoperative horn

    Tesla is recalling certain 2021-2024 Model S and 2021-2025 Model X vehicles because an airbag with the incorrect horn pad may have been installed, preventing the horn from sounding.

    Product
    TESLA — TESLA MODEL X, MODEL S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0271-2025·2025-03-19

    Duloxetine Capsules Recalled for N-Nitroso Impurity Exceeding FDA Limits

    Breckenridge Pharmaceutical is recalling 11,125 bottles of Duloxetine 20mg capsules nationwide due to N-nitroso-duloxetine impurity above FDA-recommended limits. The impurity was detected during quality control testing.

    Product
    DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0266-2025·2025-03-19

    Unisom SleepMelts Sleep-Aid Tablets Recalled for Nitrosamine Impurity

    Chattem Inc. is recalling Unisom SleepMelts diphenhydramine HCl 25 mg tablets nationwide due to a nitrosamine impurity detected above FDA's acceptable daily intake limit. Affected lots expire between May 2025 and April 2026.

    Product
    Unisom, SleepMelts, Diphenhydramine HCl tablets, 25 mg, Nighttime Sleep-Aid, 4 x 8 blister packs per carton, Cherry flavor, Manufactured by Adare Pharmaceuticals, Inc., Dist. by Chattem, Inc., P.O. Box 2219, Chattanooga, TN 37409, UPC # 0 41167 0014 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0624-2025·2025-03-19

    Green Chile Bean Burritos Recalled for Undeclared Milk Allergen

    Mi Ranchito Foods is recalling Green Chile Bean Burritos because milk is not listed in the ingredient statement, posing a risk for consumers with milk allergies.

    Product
    Green Chile Bean Burrito, 15 days refrigerated at 33 45 degrees Fahrenheit. 120 days frozen at or below 32 degrees Fahrenheit. Packaged in cellophane wrapper. Net wt. 10 ounces, UPC #21856 11136. Mi Ranchito Foods, Inc. 606 Central Avenue, Bayard, NM 88023
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1311-2025·2025-03-19

    Multiple hemostatic forceps models recalled due to clamp breakage risk

    Aesculap is recalling 1,147 hemostatic forceps due to clamp breakage risk when used beyond design specifications. Units were distributed nationwide and internationally to healthcare providers.

    Product
    Numerous models of nonsterile hemostatic forceps: (1) REF FB458R, Glover ATR.CLAMP CVD 215MM; (2) REF FB459R, Glover ATR.CLAMP CVD 245MM; (3) REF FB461R, Glover ATR.CLAMP 195MM; (4) REF FB462R, Glover ATR.CLAMP 210MM; (5) REF FB469R, Leland-Jones Peripheral CLMPSTR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1307-2025·2025-03-19

    CardiFocus Heartlight X3 Cardiac Catheter Sterile Barrier Damage Recall

    CardioFocus is recalling 833 units of CardiFocus Heartlight X3 cardiac catheters due to potential damage to the sterile barrier pouch that could compromise product sterility. Affected units were distributed worldwide.

    Product
    CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial fibrillation. It is introduced percutaneously in the setting of an Electrophysiology or Catheterization Laboratory Model: 18-5000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1322-2025·2025-03-19

    ZOLL Powerheart G5 AED Self-Test May Fail Under Extreme Environmental Conditions

    ZOLL is recalling certain Powerheart G5 AED units that may fail their self-test when exposed to extreme temperatures or humidity. The affected devices could fail to function properly in emergencies.

    Product
    Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-00A-TSO, (2) G5S-01A, (3) G5S-02A, (4) G5S-05A, (5) G5S-08A, (6) G5S-10A, (7) G5S-11A, (8) G5S-80A-TSO, (9) G5S-80-L (10) G5S-90A; Software Version: NA Product Description: The Powerheart G5…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0270-2025·2025-03-19

    Duloxetine 30mg Delayed-Release Capsules Recalled for N-Nitroso Impurity

    Breckenridge Pharmaceutical recalls 14,749 bottles of duloxetine 30mg delayed-release capsules due to N-nitroso impurity above FDA safety limits. Patients taking this medication should contact their healthcare provider to verify if their prescription is affected.

    Product
    DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0628-2025·2025-03-19

    HEB Spinach Artichoke Dip Recalled for Potential Metal Contamination in Texas

    HEB is recalling Spinach Artichoke Dip sold in Texas due to potential metal contamination. Consumers should not consume the affected products.

    Product
    " Spinach Artichoke Dip (Sold Hot) 1 lb " Spinach Artichoke Dip (Sold Cold) 1 lb " Spinach Artichoke Dip (Sold in Bulk for Customer Self Service)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0622-2025·2025-03-19

    Soup and oyster crackers recalled for potential stainless steel wire

    Multiple brands of soup and oyster crackers are being recalled due to potential stainless steel wire. The affected products were distributed across 24 states.

    Product
    1.) Market Pantry Soup & Oyster Crackers, NET WT 9 OZ (255g), packaged in flexible plastic bags, 12 count per case, Distributed By: Target Corporation, Minneapolis, MN 55403 2.) Great Value Soup & Oyster Crackers, NET WT 9 OZ (255g), packaged in flexible plastic bags, 12 count…
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-0619-2025·2025-03-19

    Van Camp's Canned Tuna Recalled for Potential Botulism Risk from Faulty Lids

    Chicken of the Sea is recalling 14,147 cases of Van Camp's Solid Light Yellowfin Tuna due to improperly secured easy-pull lids that may allow Clostridium botulinum contamination. No illnesses have been reported.

    Product
    Van Camp's branded Solid Light Yellowfin in Vegetable oil; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Distributed by: Chicken of The Sea Intl.; El Segundo, CA 90245 U.S.A. UPC# 48000 25015 UPC# 48000 75015
    Category
    Food
    Distribution
    Distributed nationwide

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