April 2025 recalls

547 recalls were announced in April 2025.

What the numbers show

Critical: 1
Severe: 125
High: 277
Moderate: 138
Low: 6

Of the 547 recalls this month scored against our rubric, 0% are Critical, 23% are Severe.

Which agencies issued them

1–100 of 547

SevereFDA (Drugs)·D-0373-2025·2025-04-30
Ketamine HCl Syringes Recalled for Lack of Sterility Assurance
Denver Solutions, LLC is recalling Ketamine HCl 50mg per 5mL single-dose syringes nationwide due to leaking or damaged syringes that may lack sterility assurance. Two affected lots are identified with expiration dates in July 2025.
Product
Ketamine HCl 50mg per 5mL (10 mg per mL), 5mL Single Dose Syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112.NDC: 71449-068-11
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1643-2025·2025-04-30
Amplatzer TorqVue LP Delivery System Recall for Shaft Breach
Abbott is recalling specific lots of the Amplatzer TorqVue LP Delivery System due to a possible small breach in the shaft that is not visible but could lead to prolonged procedures, blood loss, or air embolism.
Product
Amplatzer TorqVue LP Delivery System (TVLP), Model nos. 9-TVLP4F90/060 and 9-TVLP4F90/080
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0723-2025·2025-04-30
Zaarah Herbals Vasaka Powder Recalled for Elevated Lead Content
Zaarah Herbals brand Vasaka Powder is recalled due to elevated lead levels of 6.504 ppm. The product was distributed in New York, Connecticut, New Jersey, and California.
Product
Zaarah Herbals brand Vasaka Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 99967 0
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0730-2025·2025-04-30
Walker's Wine Juice Pumpkin Juice recalled for potential botulinum contamination
Walker's Wine Juice Pumpkin Juice in 2.5, 5, 30, 60, and 275 gallon bulk containers is being recalled due to potential contamination with Clostridium botulinum. The product was distributed across multiple states.
Product
Walker's Wine Juice Pumpkin Juice 2.5, 5, 30, 60, 275 gallon bulk containers
Category
Food
Distribution
12 states
SevereFDA (Food)·F-0722-2025·2025-04-30
Zaarah Herbals Gurmar Powder recalled for elevated lead levels
Zaarah Herbals brand Gurmar Powder is being recalled due to elevated lead levels. The product was distributed in New York, Connecticut, New Jersey, and California.
Product
Zaarah Herbals brand Gurmar Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 99969 4
Category
Food
Distribution
4 states
SevereFDA (Devices)·Z-1644-2025·2025-04-30
Amplatzer TorqVue LP Catheter Recalled for Shaft Breach Risk
Abbott is recalling the Amplatzer TorqVue LP Catheter (Model 9-TVLPC4F90/080) due to a potential small breach in the proximal shaft that may not be visible and could lead to prolonged procedures, blood loss, or air embolism.
Product
Amplatzer TorqVue LP Catheter (TVLPC), Model no. 9-TVLPC4F90/080
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0368-2025·2025-04-30
Haloperidol Decanoate Injection Recalled for Lack of Sterility Assurance
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility and bacterial contamination detected in some media fill units. The affected product was distributed nationwide.
Product
HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0369-2025·2025-04-30
Haloperidol Decanoate Injection Recalled Due to Sterility Concerns
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection vials nationwide because some media fill units showed bacterial contamination, indicating a lack of sterility assurance. The affected product is a 100mg/mL injectable antipsychotic medication.
Product
HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0371-2025·2025-04-30
Dexmedetomidine HCl Syringes Recalled for Potential Sterility Issue
Leiters Health is recalling dexmedetomidine HCl PF syringes nationwide due to leaking or damaged syringes that may not maintain sterility. Affected lot 2431276A has an expiration date of 4/20/2025.
Product
dexmedeTOMIDine HCl PF, in 0.9% Sodium Chloride, 20 mcg (base) per 5mL, (4 mcg (base) per mL), 5mL Single Dose syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112, NDC: 71449-131-11.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0374-2025·2025-04-30
Rocuronium Bromide Syringes Recalled Due to Sterility Assurance Risk
Denver Solutions, LLC DBA Leiters Health is recalling Rocuronium Bromide 50 mg per 5mL syringes due to potential leaking or damage that may compromise sterility assurance.
Product
Rocuronium Bromide 50 mg per 5mL (10mg per mL), 5mL Single Dose Syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC: 71449-004-11
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1585-2025·2025-04-30
Novasight Hybrid Catheter Recalled for Potential Sheath Detachment
Conavi Medical Inc. is recalling the Novasight Hybrid Catheter (Model TA-06-0001) due to manufacturing issues that could cause the catheter sheath to detach. The device is used for diagnostic intravascular imaging.
Product
Brand Name: Novasight Hybrid System Product Name: Novasight Hybrid Catheter Model/Catalog Number: TA-06-0001 Product Description: Common Name: Diagnostic intravascular catheter Description: The Novasight Hybrid catheter is a 3Fr single use, sterile device, which will be able
Category
Medical Device
Distribution
4 states
SevereFDA (Food)·F-0724-2025·2025-04-30
Zaarah Herbals Rasayan Churan Recalled for Elevated Lead Levels
Zaarah Herbals brand Rasayan Churan (100g jars) is recalled due to elevated lead levels of 88.038 ppm. The product was distributed in New York, Connecticut, New Jersey, and California.
Product
Zaarah Herbals brand Rasayan Churan; packaged in 100g clear jars with gold lids; UPC:6 35028 99966 3
Category
Food
Distribution
4 states
SevereFDA (Drugs)·D-0372-2025·2025-04-30
PHENYLephrine HCl Injection Syringes Recalled for Lack of Sterility
Denver Solutions, LLC DBA Leiters Health is recalling PHENYLephrine HCl 0.5 mg per 5mL single-dose syringes because some syringes may be leaking or damaged, which could compromise sterility assurance.
Product
PHENYLephrine HCl in 0.9% Sodium Chloride, 0.5 mg per 5mL (100 mcg/mL), 5 mL Single Dose Syringe, Rx Only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC: 71449-001-11,
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0367-2025·2025-04-30
Haloperidol Decanoate Injection Recalled Due to Sterility Concerns
Amerisource Health Services LLC is recalling Haloperidol Decanoate Injection due to lack of assurance of sterility and bacterial contamination detected in some media fill units. The drug is used for intramuscular injection to treat psychiatric conditions.
Product
HALOPERIDOL DECANOATE — HALOPERIDOL DECANOATE (HALOPERIDOL DECANOATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0721-2025·2025-04-30
Zaarah Herbals Bhringraj Powder Recalled for Elevated Lead and Arsenic
Zaarah Herbals brand Bhringraj Powder contains elevated levels of lead and arsenic. Consumers should not use the product and should contact the recalling firm for instructions.
Product
Zaarah Herbals brand Bhringraj Powder; packaged in 100g clear jars with gold lids; UPC: 6 35028 99973 1
Category
Food
Distribution
4 states
HighFDA (Drugs)·D-0370-2025·2025-04-30
Glycopyrrolate 1mg/5mL Syringes Recalled for Sterility Risk
Denver Solutions, LLC (DBA Leiters Health) is recalling Glycopyrrolate 1mg/5mL single-dose syringes (Lot #2431015B, expiration 4/10/2025) distributed nationwide because some syringes were found to be leaking or damaged, which compromises sterility assurance.
Product
Glycopyrrolate, 1mg per 5mL, (0.2 mg/mL), Single Dose 5 mL syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC 71449-104-11
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1623-2025·2025-04-30
Medtronic NIM Vital Nerve Monitoring System Software Version Recall
Medtronic is recalling NIM Vital Nerve Monitoring Systems with software versions v1.6.4 or earlier due to potential increased stimulus artifact that may require troubleshooting and could lead to procedure delay, extubation, and medical intervention.
Product
NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0, REF: NIM4CM01; CONSOLE NIM4CM01RF NIM 4.0 REFURBISHED, REF: NIM4CM01RF; PATIENT INTERFACE NIM4CPB1 NIM 4.0, REF: NIM4CPB1; PATIENT INTFC NIM4CPB1RF NIM 4.0 REFURB, REF: NIM4CPB1RF; SOFTWARE NIM4SWU143 UPGRA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1653-2025·2025-04-30
CELL-DYN Ruby hematology analyzer expiration date software defect
Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers because a software defect allows expired reagents to be used without user notification. The system may incorrectly update expiration dates to current or future dates, contrary to the operator's manual.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-03 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1654-2025·2025-04-30
Abbott CELL-DYN Ruby hematology analyzer affected by expired reagent date masking
Abbott is recalling the CELL-DYN Ruby hematology analyzer because expired reagents may have their expiration dates automatically changed to current or future dates without user notification, potentially leading to use of expired reagents.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-10 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1622-2025·2025-04-30
VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System C-Ring Break
Maquet Cardiovascular is recalling the VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System due to a ceramic C-Ring component that may break during use. At least 12 user complaints were reported as of March 3, 2025.
Product
The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm extended length endoscope. The Harvesting Cannula has four lumens which house the endoscope, C-Ring, distal lens washer tube, and Harvesting Tool for cutting and cauterizin
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1656-2025·2025-04-30
CELL-DYN Ruby hematology analyzer medical device recall
Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers because expired reagents may be used without user notification when scanned or manually entered into the system, contrary to manufacturer guidelines.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 04U42-84 Software Version: All software versions Product Description: CELL-DYN Ruby
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1583-2025·2025-04-30
Zenition 70 Medical Device Recall: Unintended Radiation Exposure Risk
Philips is recalling Zenition 70 systems with Vascular Extension option and Wireless Foot Switch due to potential for unintended radiation exposure in healthcare facilities.
Product
Zenition 70. The device is to be used in health care facilities both inside and outside the operating room, sterile as well as non-sterile environment in a variety of procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0733-2025·2025-04-30
Magic Flame Hulled Sunflower Kernels Bakery Grade Recall
JJ Nuts, LLC is recalling Magic Flame Hulled Sunflower Kernels due to glass fragments found in the finished product.
Product
MAGIC FLAME, HULLED SUNFLOWER KERNELS, BAKERY GRADE, 501b. Bag, Three ply Paper bags, 1100 Paper bags x 50 Ib. on 20 pallets. Store in dry warehouse, room temperature
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1669-2025·2025-04-30
Rover Mobile X-ray System internal fastening mechanism failure potential
Micro-X Ltd. is recalling Rover Mobile X-ray System units (models MXU-RV71, MXU-RV35) due to a potential failure of the internal fastening mechanism within the generator. Affected units were distributed in New Jersey, Washington, and Puerto Rico.
Product
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71, MXU-RV35 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates a self-contained X-ray generator, imaging display and software for acquiring med
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-1580-2025·2025-04-30
Zenition 50 Medical Imaging Devices Wireless Foot Switch Recall
Philips is recalling Zenition 50 medical imaging devices because the wireless foot switch pedal may get stuck in the active position, causing unintended radiation emission.
Product
Zenition 50. Product Code 718096. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the devices.
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0720-2025·2025-04-30
Chicken Salad Recalled Due to Undeclared Milk Allergen
Cromer Food Services is recalling chicken salad sandwiches because milk was not declared on the label. Consumers with milk allergies are at risk.
Product
CFS CROMER FOOD SERVICES, INC. Anderson, SC 29621 CHICKEN SALAD On White NET WT. 4.3 OZ CONTAINS: EGGS, WHEAT, SOY UPC 31166 & UPC 13172
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1652-2025·2025-04-30
CELL-DYN Ruby Hematology Analyzer Expiration Date Software Defect
Abbott's CELL-DYN Ruby hematology analyzer may accept expired reagents without alerting the operator, potentially allowing use of expired materials in patient testing.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-01 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1655-2025·2025-04-30
CELL-DYN Ruby hematology analyzer system expiration date validation
Abbott Laboratories is recalling CELL-DYN Ruby hematology analyzers (model 08H67-13) because expired reagents can be used without proper notification when their expiration dates are scanned or entered into the system.
Product
Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number: 08H67-13 Software Version: All software versions Product Description: CELL-DYN Ruby Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1663-2025·2025-04-30
Skytron Freedom Monitor Mount Hardware Recall for Inadequate Thread Engagement
The mounting hardware supplied with the Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount does not provide adequate thread engagement to support the weight of the frame and monitor, creating a risk of hardware failure and separation.
Product
Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0734-2025·2025-04-30
S Martinelli Apple Juice Recalled for Potential Patulin Contamination
S Martinelli & Company is recalling approximately 7,234 cases of apple juice in 10 oz bottles due to potential contamination with patulin. Consumers who have purchased affected product should not consume it.
Product
Apple Juice; clear/translucent bulbous/round glass bottle with white metal screw top lid; (4 - 10 oz bottles per pack; 6 packs per case)
Category
Food
Distribution
28 states
HighFDA (Devices)·Z-1651-2025·2025-04-30
Stryker Latitude EV Humeral Revision Stem Trial with Incorrect Marking
A specific lot of Stryker Latitude Humeral Trial Stems has incorrect laser marking and color indicator, potentially resulting in implantation of the wrong device size and orientation.
Product
stryker Latitude EV HUMERAL REVISION STEM TRIAL, L: 150mm, Size: LARGE, Side: RIGHT, REF 9030103; Prosthesis, Elbow, Semi-Constrained, Cemented
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0737-2025·2025-04-30
Cuban-Style Black Bean Soup recalled for potential wood contamination
Request Foods Incorporated is recalling Cuban-Style Black Bean Soup due to potential contamination with wood. The product was distributed in Illinois and Michigan.
Product
Cuban-Style Black Bean Soup, 4 / 4lb pouches, Net Wt. 16lb
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1639-2025·2025-04-30
BD PYXIS MEDBANK Automated Dispensing Cabinet Software Defect
CareFusion's BD PYXIS MEDBANK and MEDFLEX automated dispensing cabinets may experience a software issue during bin restocking that doubles bin quantities, potentially delaying access to medications and supplies.
Product
BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI 1HH-1HM-1FM, 169-102; MINI 2FH, 138902-01; MINI 2FH, 169-104; MINI 2FM, 169-105; MINI 2HH-1FH, 169-106; MINI 2HH-1FH, 138908-01; MINI 2HH-1FM, 169-107; MINI
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1650-2025·2025-04-30
InPen Smart Insulin Pen Recall Due to Incorrect Assembly
Medtronic MiniMed is recalling InPen smart insulin pens that may have been incorrectly assembled, potentially causing the insulin cartridge to not fit or the cartridge holder to be difficult to remove. Users without backup insulin could experience temporary hyperglycemia.
Product
InPen smart insulin pen, REF: MMT-105NNBLNA, MMT-105NNGYNA, MMT-105NNPKNA, MMT-105ELBLNA, MMT-105ELGYNA, MMT105ELPKNA
Category
Medical Device
Distribution
41 states
HighFDA (Devices)·Z-1582-2025·2025-04-30
Veradius Unity wireless foot switch pedal may emit unintended radiation
Philips North America is recalling Veradius Unity foot switch pedals that may become stuck in the active position, causing unintended radiation emission during medical procedures.
Product
Veradius Unity. Product Code 718132. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the devices.
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0732-2025·2025-04-30
MO-CHA Premium Non-Dairy Creamer Recalled for Undeclared Milk Allergen
MO-CHA brand Premium Non-Dairy Creamer is recalled because the label does not declare milk as an allergen, despite milk being present in the product. Consumers with milk allergies are at risk of adverse reaction.
Product
MO-CHA brand Premium Non-Dairy Creamer; INGREDIENTS Glucose syrup, Refined vegetable oil, Whey powder, Sugar, Casein, Emulsifier (471, 481i), Stabilizer(340ii, 452i), Anti-caking agent(551), Food flavor; Shelf Life: 24 months; Net Weight (NET WT): 2.2 lbs (1kg); IMPORTED BY Momo
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-1670-2025·2025-04-30
Rover Mobile X-ray System internal fastening mechanism failure risk
Micro-X Ltd. is recalling the Rover Mobile X-ray System (model MXU-RV35) due to a potential failure of the internal fastening mechanism within the generator. Five units distributed in New Jersey, Washington, and Puerto Rico are affected.
Product
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:MXU-RV35 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates a self-contained X-ray generator, imaging display and software for acquiring medical diagno
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-1581-2025·2025-04-30
Zenition 70 Radiological System Wireless Foot Switch Recall
Philips is recalling Zenition 70 radiological systems with wireless foot switches that may stick in the active position when released, potentially causing unintended radiation emission during medical procedures.
Product
Zenition 70. Product Code 718133. The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the devices.
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0729-2025·2025-04-30
Spermidine Dietary Supplement Recalled for Undeclared Wheat Allergen
Supplement Manufacturing Partner Inc. is recalling Spermidine Maximum Strength 10 mg dietary supplement (Lot 12792402-44) because it contains undeclared wheat, a major allergen not listed on the label.
Product
Spermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 Capsules, oral consumption, shelf life: 24 months, PETE/White/150cc Plastic bottle/lid, 120 count.Supplement Facts: Spermidine 3HCL 10mg*** Other Ingredients: Hydroxypropyl Methylcellu
Category
Drug
Distribution
0 states
HighFDA (Devices)·Z-1660-2025·2025-04-30
Philips Brilliance CT Big Bore X-Ray System Gantry Motion Collision Hazard
Philips is recalling Brilliance CT Big Bore computed tomography systems due to unintended motion in the interventional control that may cause the gantry or table to collide with operators or patients.
Product
Philips Brilliance CT Big Bore, Software Version 4.8.0.10430. Computed Tomography X-Ray System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1657-2025·2025-04-30
Globus Medical MAGEC 2 Rod recalled for incorrect outer diameter assembly
Globus Medical is recalling MAGEC 2 Rod model MC2-5090S devices because certain units were assembled with a 5.5mm outer diameter rod instead of the required 5.0mm specification.
Product
MAGEC 2 Rod, 5.0mm 90mm Standard; Version/Model: MC2-5090S;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1647-2025·2025-04-30
Zimmer Biomet Ceramic Hip Prosthesis Heads Lack Stem Compatibility Information
Zimmer, Inc. is recalling Zimmer Biomet Ceramic Head hip prostheses (Model 802802201, 22.2 mm diameter) because product labeling does not adequately provide compatibility information for use with cobalt-chrome or stainless-steel femoral stems.
Product
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, -3 Neck, Model Number 802802201; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1641-2025·2025-04-30
Merit Medical EsophyX Z+ Fastener Delivery Device Instructions Update
Merit Medical has updated instructions for the EsophyX Z+ fastener delivery device to provide additional information about risks associated with device over-rotation and multiple fastener deployment.
Product
Merit Medical , REF: R2275, EsophyX Z+ with SerosaFuse Implantable Fasteners, (1) Fastener Delivery Device, (2) 7.5mm Cartridges, STERILEEO,RxOnly
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1664-2025·2025-04-30
Beckman Coulter DxI 9000 Access Immunoassay Analyzer communication loss
Beckman Coulter DxI 9000 Access Immunoassay Analyzer may lose connection to laboratory information systems, interrupting sample processing and delaying patient test results.
Product
Beckman Coulter DxI 9000 Access Immunoassay Analyzer
Category
Medical Device
Distribution
0 states
ModerateFDA (Food)·F-0731-2025·2025-04-30
Gold Garlic Powder Irradiated Recalled for Potential Metal Contamination
Pacific Meridian Group, LLC is recalling Gold Garlic Powder Irradiated due to potential contamination with foreign objects (metal). The recalled product was distributed in CA, IL, and TX.
Product
GOLD GARLIC POWDER IRRADIATED; NET WT. 50 LBS; PRODUCT OF CHINA
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0727-2025·2025-04-30
Texas Olive Company Capers Capote recalled due to contamination risk
Texas Olive Company Capers Capote in 8 oz. plastic containers and 16 oz. glass jars is being recalled because the repacking and sealing methods pose a possible risk of contamination.
Product
Texas Olive Company Capers Capote 8 oz. plastic containers. All lots with expiry prior to 06/04/2025 Texas Olive Company Capers Capote 16 oz. glass jar. All lots with expiry prior to 12/21/2025
Category
Food
Distribution
2 states
ModerateFDA (Drugs)·D-0377-2025·2025-04-30
Clomipramine Hydrochloride Capsules recalled for degradation product specification failure
Lupin Pharmaceuticals is recalling Clomipramine Hydrochloride Capsules (25 mg) due to an unspecified degradation product detected in stability testing. The defect was identified during an 18-month long-term stability study.
Product
CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE CAPSULES)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0739-2025·2025-04-30
IQF Cilantro Large Recalled Due to Foreign Object Contamination
Supherb Farms is recalling frozen cilantro (IQF Cilantro Large, 30 lb packages) distributed across the United States, Canada, and Mexico due to potential contamination with foreign objects.
Product
Label: IQF CILANTRO LARGE; NET WT: 30LB; PERISHABLE KEEP FROZEN; Packaging: blue plastic liner inside brown cardboard box
Category
Food
Distribution
8 states
ModerateFDA (Food)·F-0735-2025·2025-04-30
Moroccan Style Lentil Soup recalled for potential wood contamination
Request Foods Incorporated is recalling Moroccan Style Lentil Soup due to potential contamination with wood fragments. The product was distributed in Illinois and Michigan.
Product
Moroccan Style Lentil Soup, 4 x 8lb pouches, Net wt. 32lb
Category
Food
Distribution
2 states
ModerateFDA (Food)·F-0740-2025·2025-04-30
Frozen Chopped Cilantro Recalled for Potential Foreign Object Contamination
Supherb Farms is recalling frozen chopped cilantro due to potential contamination with foreign objects. Consumers should not use the product and should discard it or return it to the retailer.
Product
Label: FROZEN CHOPPED CILANTRO; PACK SIZE: 4 - 8 oz; NET WT: 2 lb; PERISHABLE - KEEP FROZEN; Packaging: 4 - 8 oz ziploc plastic bags in a white cardboard box; Net Wt. 2 lb
Category
Food
Distribution
8 states
ModerateFDA (Food)·F-0726-2025·2025-04-30
Texas Olive Co. Pepperoncini 16 oz Glass Jars Recalled
All American Trading Of Houston, Inc. is recalling Texas Olive Co. Pepperoncini 16 oz glass jars due to potential contamination from non-heat-sealed sealing methods. The recall affects products sold in Texas and Mississippi.
Product
Texas Olive Co. Pepperoncini 16 oz glass jars
Category
Food
Distribution
2 states
ModerateFDA (Drugs)·D-0375-2025·2025-04-30
Hemopropin Ointment Recalled Due to Manufacturing Process Deviations
Apipharma is voluntarily recalling Hemopropin Ointment due to Current Good Manufacturing Practice (CGMP) deviations identified during manufacturing. The recall affects specific lot numbers distributed in Arizona.
Product
Hemopropin Ointment, Lanolin 17.76% and Petrolatum 71.2%, Net Wt. 0.7 oz (20g) tubes, Manufactured by: Apipharma d.o.o, Croatia, Distributed by: Apipharma, LLC, Tempe, AZ UPC 3 858882 103534 and UPC 3 858882 101318
Category
Drug
Distribution
1 state
ModerateFDA (Devices)·Z-1640-2025·2025-04-30
Merit Medical EsophyX Z+ Fastener Delivery Device Safety Update
Merit Medical is updating instructions for the EsophyX Z+ Fastener Delivery Device due to risks associated with device over-rotation and multiple fastener deployment.
Product
Merit Medical, REF: R2007, EsophyX Z+, (1) Fastener Delivery Device, SterileEO, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1649-2025·2025-04-30
Zimmer Biomet Ceramic Hip Head 22.2 mm Lacks Stem Compatibility Information
Zimmer, Inc. is recalling a ceramic hip prosthesis head because the product labeling does not adequately describe compatibility with certain femoral stems used in hip replacement surgery.
Product
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +3 Neck, Model Number 802802203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0736-2025·2025-04-30
Mexican Street Corn Soup recalled for possible wood contamination
Request Foods Incorporated is recalling Mexican Street Corn Soup due to potential contamination with foreign material (wood). The product was distributed in Illinois and Michigan.
Product
Mexican Street Corn Soup, 4 / 4lb pouches, Net Wt. 16lb
Category
Food
Distribution
2 states
ModerateFDA (Devices)·Z-1645-2025·2025-04-30
Zimmer Biomet Ceramic Hip Prosthesis Head Lacks Stem Compatibility Information
Zimmer, Inc. is recalling a ceramic hip prosthesis head because its labeling does not adequately describe compatibility with cobalt-chrome or stainless-steel femoral stems.
Product
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +0 Neck, Model Number 802602202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1666-2025·2025-04-30
Tempus Pro Patient Monitor software error when using video laryngoscope
Remote Diagnostic Technologies Ltd. is recalling Tempus Pro Patient Monitors due to a software issue that causes an error screen when a video laryngoscope is attached to the device.
Product
Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007 (Tempus Pro non-printer, IBP, with headset dock), 00-1024-R (Tempus Pro printer), 00-1026-R (Tempus Pro printer, IBP), 00-1007 [(Tempus Pro, BT Dock (IB Only)],
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1665-2025·2025-04-30
Alinity m System nucleic acid testing instruments recalled for liquid spillage
Abbott Molecular is recalling the Alinity m System due to a design flaw that may allow liquid waste or system solutions to spill beyond the instrument footprint into the user's walking path.
Product
The Alinity m System is designed to automate the steps for nucleic acid testing. Model Numbers included in this recall are 08N53-001, 08N53-002, and 08N53-032 (Refurbished).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0728-2025·2025-04-30
Texas Olive Company Giardiniera 16 oz. glass jars recalled
All American Trading Of Houston, Inc. is recalling Texas Olive Company Giardiniera in 16 oz. glass jars with expiry dates prior to 06/14/2025 due to non-heat-sealed repacking methods that pose a possible contamination risk.
Product
Texas Olive Company Giardiniera 16 oz. glass jars All lots with expiry prior to 06/14/2025
Category
Food
Distribution
2 states
ModerateFDA (Devices)·Z-1648-2025·2025-04-30
Zimmer Biomet Ceramic Hip Prosthesis Head Lacks Compatibility Labeling
Zimmer, Inc. is recalling a ceramic femoral head for hip prosthesis (Model 802802202, 22.2 mm) because product labeling does not adequately describe compatibility with certain metal femoral stems.
Product
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, Type 1, +0 Neck, Model Number 802802202; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0738-2025·2025-04-30
Beecher's Street Corn recalled for potential wood contamination
Request Foods Incorporated is recalling Beecher's Street Corn (18oz) due to potential contamination with wood foreign material. Affected products were distributed in Illinois and Michigan.
Product
Beecher's Street Corn, 18oz, 8 retail units per case, UPC 782045 115009
Category
Food
Distribution
2 states
ModerateFDA (Drugs)·D-0384-2025·2025-04-30
Urodel Homeopathic Urinary Tract Infection Relief Tablets Recalled
Pharmadel, LLC is recalling Urodel homeopathic chewable tablets for urinary tract infection symptom relief due to cGMP manufacturing deviations. The voluntary recall affects 10,752 bottles distributed in Delaware.
Product
Urodel, Urinary Tract Infection Symptoms Relief, Homeopathic, 30 chewable tablets per bottle, Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-406-30
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0381-2025·2025-04-30
Kingskin Salicylic Acid Wart Removal Recall Due to cGMP Deviations
Pharmadel, LLC is recalling Kingskin salicylic acid wart-removal solution due to cGMP manufacturing deviations. The recall affects 20,048 bottles distributed in Delaware.
Product
KINGSKIN — KINGSKIN (SALICYLIC ACID)
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0383-2025·2025-04-30
Rapidol Arnica Tablets recalled due to manufacturing deviations
Pharmadel is recalling 6,048 bottles of Rapidol Arnica Tablets homeopathic medicine due to current good manufacturing practice (cGMP) deviations. The recall affects bottles with lot EAT-01, expiration date March 27, distributed in Delaware.
Product
Rapidol Arnica Tablets, Homeopathic Medicine, 100-count bottle, Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-405-99
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0385-2025·2025-04-30
HYDROmorphone Hydrochloride 50 mg Cassettes Recalled for Superpotency
OurPharma LLC is recalling HYDROmorphone Hydrochloride 50 mg/50 mL cassettes nationwide because the assay results showed higher potency than specification.
Product
HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL), packaged in a 50 mL Cassette, Rx Only, OurPharma, LLC, 2512 S. City Lake Rd., Fayetteville, AR 72701, NDC 73013-1040-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0379-2025·2025-04-30
DoloDent Maximum Strength Toothache Drops Recalled for cGMP Deviations
Pharmadel, LLC is recalling DoloDent Maximum Strength Toothache Drops due to current Good Manufacturing Practice (cGMP) deviations. The voluntary recall affects 9,504 bottles distributed in Delaware.
Product
DoloDent Maximum Strength Toothache Drops, Homeopathic Oral Drops, 0.50 oz fl (15 mL), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-400-15
Category
Drug
Distribution
1 state
ModerateFDA (Devices)·Z-1646-2025·2025-04-30
Zimmer Biomet Ceramic Femoral Head Hip Prosthesis Labeling Recall
Zimmer, Inc. is recalling a ceramic femoral head hip prosthesis (Model 802602203) because product labeling lacks compatibility information for use with cobalt-chrome or stainless-steel femoral stems.
Product
Zimmer Biomet Ceramic Head, 22.2 mm Diameter, 12/14 Taper, +3 Neck, Model Number 802602203; Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented or Non- Porous, Uncemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0380-2025·2025-04-30
DoloEar Homeopathic Earache Drops Recalled for cGMP Deviations
Pharmadel, LLC is recalling DoloEar Homeopathic Earache Drops (0.50 oz, 15 mL) due to cGMP (current Good Manufacturing Practice) deviations. The recall affects 27,648 bottles distributed in Delaware.
Product
DoloEar Earache Drops, Homeopathic, 0.50 oz fl (15 mL), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-401-15
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0382-2025·2025-04-30
Rapidol Arnica Gel topical homeopathic medicine recalled for manufacturing violations
Pharmadel, LLC is recalling Rapidol Arnica Gel (2 oz, 57 g) distributed in Delaware due to manufacturing process deviations. The voluntary recall affects 6,048 bottles of lot EAG-01 with expiration date MAR 27.
Product
Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine, 2 oz (57 g), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-403-02
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0386-2025·2025-04-30
Bimatoprost Bulk Powder Recalled by Medisca for CGMP Deviations
Medisca Inc. is voluntarily recalling Bimatoprost bulk powder in three sizes due to manufacturing process deviations. The powder was distributed nationwide.
Product
Bimatoprost powder, Bulk Ingredient, a) 5g (NDC 38779-3066-03), b) 1g (NDC 38779-3066-06), c) 1g (NDC 38779-3066-09) drums, Medisca, Plattsburgh, NY
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0388-2025·2025-04-30
Duloxetine Delayed-Release Capsules Recalled for Nitrosamine Impurity
Breckenridge Pharmaceutical is recalling Duloxetine Delayed-Release Capsules 30 mg nationwide due to the presence of a nitrosamine drug substance related impurity above proposed interim limits.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0376-2025·2025-04-30
Kapsin Ointment Drug Recalled Due to Manufacturing Process Deviations
Apipharma is voluntarily recalling Kapsin Ointment (Camphor 3.16% and Capsaicin 0.03%) distributed in Arizona due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Kapsin Ointment, Camphor 3.16% and Capsaicin 0.03%. Net Wt. 2 oz (60g) tubes, Manufactured by: Apipharma d.o.o, Jeronima Kavanjina 26, 10090 Zagreb, Croatia, Distributed by: Apipharma, LLC, 2331 West Alameda Drive, Tempe, AZ 85282 UPC 3 858882 101363
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0387-2025·2025-04-30
Duloxetine delayed-release capsules recalled for nitrosamine impurity
Breckenridge Pharmaceutical is recalling Duloxetine 60 mg delayed-release capsules nationwide due to elevated levels of a nitrosamine-related impurity that exceed the FDA's interim safety limit. The affected lots include bottles with expiration dates in April 2027.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0378-2025·2025-04-30
Clindamycin HCl 300 mg Capsule Recalled for CGMP Deviations
RemedyRepack Inc. is recalling Clindamycin HCl 300 mg Capsules due to current Good Manufacturing Practice (CGMP) deviations. The recall affects approximately 1,858 30-count blister cards distributed in Pennsylvania.
Product
Clindamycin HCl, 300 mg Capsule, QTY: 30 Capsules per bottle, Rx Only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701. NDC; 70518-3772-00
Category
Drug
Distribution
1 state
ModerateFDA (Devices)·Z-1659-2025·2025-04-30
Radiometer ABL90 Series Blood Analyzers May Unexpectedly Freeze
Radiometer ABL90 FLEX and ABL90 FLEX PLUS analyzers running Windows 10 versions RWIN10 1.0 and RWIN10 1.1 may freeze unexpectedly during sample measurement, causing test results to be lost and delayed.
Product
Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090 Radiometer ABL90 Series - Radiometer ABL90 FLEX PLUS Model Number 393-092 The Radiometer ABL90 Series is a portable, automated analyzer for use in the laboratory environment, near patients or point-of-care
Category
Medical Device
Distribution
49 states
LowFDA (Devices)·Z-1658-2025·2025-04-30
Edge Biologicals Sterile Water incorrectly labeled product packaging
Edge Biologicals is recalling Sterile Water, 3mL (Product Number T-0780, Lot 01223) due to incorrect labeling on the product's outer packaging. The affected units were distributed nationwide in Pennsylvania.
Product
Edge Biologicals STERILE WATER, 3ML, 100/PK CAT T-0780 Sterile Water, 3mL, 10/PK - Sterile water is used in making dilutions of samples/transport media in preparation for microbial testing of the sample. It is also used for diluting sterile reagents and microorganism preparat
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1671-2025·2025-04-30
Straumann WB XL Anatomic Healing Abutment XC Dental Implants
Straumann USA LLC is recalling 1,786 units of WB XL Anatomic Healing Abutment XC endosseous dental implant abutments due to incorrect blister labeling. The product was distributed worldwide.
Product
WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V011000·2025-04-29
Jeep Cherokee Recall: Power Transfer Unit Defect May Cause Loss of Drive
Chrysler is recalling 2017-2019 Jeep Cherokee vehicles because a power transfer unit defect may cause loss of drive power or park function, increasing crash risk.
Product
JEEP — JEEP CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·013-2025·2025-04-29
Smith Packing Recalls Sausage and Sliced Meat Due to High Sodium Nitrite Levels
Smith Packing, LLC is recalling approximately 18,792 pounds of ready-to-eat sausage and sliced meat and poultry products due to sodium nitrite levels exceeding regulatory limits.
Product
Smith Packing, LLC — Smith Packing, LLC Recalls Sausage and Sliced Meat and Poultry Products Due to Sodium Nitrite Levels in Excess of Regulatory Limit
Category
Food
Distribution
1 state
SevereNHTSA·25V279000·2025-04-29
Temsa Recalls TS30, TS35, and TS45 Buses Due to Brake Overheating Risk
Temsa is recalling 2021-2026 TS30, TS35, and TS45 buses because a temporary bus stop valve may activate unintentionally, causing brakes to overheat and increasing fire risk.
Product
TEMSA — TEMSA TS45, TS35, TS30
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25E031000·2025-04-29
Dainese Recalls AGV DOT Tourmodular Helmets Due to Chin Guard Defect
Dainese is recalling AGV DOT Tourmodular helmets because the chin guard plate may break, allowing the helmet to loosen or detach during a crash.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·25E030000·2025-04-28
Joyson Curtain Air Bag Inflator Recall for Rupture Risk
Key Safety Systems (Joyson) is recalling side curtain air bag inflators that may rupture due to a manufacturing defect, potentially causing injury to occupants.
Product
AIR BAGS:SIDE/WINDOW:CURTAIN:INFLATOR recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V217000·2025-04-28
Isuzu Recalls 2025 NRR EV Trucks Due to Cooling Pump Failure Risk
Isuzu is recalling 73 2025 NRR EV trucks because incompatible coolants may cause the cooling pump to fail, potentially leading to a loss of drive power and increased crash risk.
Product
ISUZU — ISUZU NRR EV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25E029000·2025-04-25
Zoox Recalls Robotaxis Due to Software Crash Risk
Zoox is recalling 2024 robotaxis because a software defect may cause the vehicle to fail to avoid a crash when another vehicle stops perpendicularly.
Product
ZOOX — ZOOX ZOOX ROBOTAXI
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V278000·2025-04-25
Forest River Bus Recalls Transit Buses Due to Wiring Fire Risk
Forest River Bus is recalling 453 transit buses because an incorrectly connected entry door ground wire may increase the risk of a fire.
Product
FOREST RIVER BUS — FOREST RIVER BUS, GLAVAL BUS CHAMPION BUS, UNIVERSAL, GLAVAL ENTOURAGE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25E028000·2025-04-25
Carrier Recalls Aspen Auxiliary Power Units Due to Fire Risk
Carrier is recalling specific Aspen Auxiliary Power Units because corrosion on the positive terminal block may cause a short circuit and increase the risk of a fire.
Product
EQUIPMENT recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V280000·2025-04-25
Polestar 2 rearview camera may not display when reversing
Polestar is recalling certain 2021-2025 Polestar 2 vehicles because the rearview camera image may not display when the vehicle is placed in reverse, failing FMVSS 111.
Product
POLESTAR — POLESTAR POLESTAR 2
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V277000·2025-04-25
Forest River Recalls 2025 Stealth and XLR Fifth Wheels for Wiring Defect
Forest River is recalling 2025 Stealth and XLR fifth wheel travel trailers because a front exterior lamp wire lacks proper circuit protection, increasing fire risk.
Product
FOREST RIVER — FOREST RIVER STEALTH, XLR TOYHAULER 5TH WHEEL
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·012-2025·2025-04-24
ACC Central Kitchen Recalls Pork Bun Products Due to Undeclared Sesame
ACC Central Kitchen LLC is recalling approximately 64,008 pounds of pork bun products because they contain sesame, an undeclared allergen. The products were shipped to retail locations in New York.
Product
ACC Central Kitchen LLC — ACC Central Kitchen LLC Recalls Pork Bun Products Due To Misbranding and Undeclared Allergens
Category
Food
Distribution
1 state
SevereCPSC·25232·2025-04-24
LED Strip Lights Recalled for Coin Battery Ingestion Hazard
AliExpress-sold RGB LED strip lights are recalled because children can easily access the coin batteries inside, creating a serious ingestion hazard. Swallowed batteries can cause severe internal burns and death.
Product
LED Strip Lights
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·25V275000·2025-04-24
2025 Can-Am Origin and Pulse Electric Motorcycle Battery Recall
NHTSA is recalling 2025 Can-Am Origin and Pulse electric motorcycles because a faulty breather valve may allow water into the battery, risking fire or loss of power.
Product
CAN-AM — CAN-AM ORIGIN, PULSE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V274000·2025-04-24
GM 6.2L V8 connecting rods and crankshafts may have manufacturing defects
General Motors is recalling certain 2021-2024 Escalade, Silverado 1500, Suburban, Tahoe, Sierra 1500, Yukon and Yukon XL vehicles with 6.2L V8 engines because connecting rod or crankshaft defects can cause engine failure.
Product
CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE ESV, ESCALADE, SUBURBAN, YUKON XL
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25239·2025-04-24
Huffy Torex 24V UTV Ride-On Toys Recalled for Fire Hazard
Huffy Corporation recalled about 24,700 Torex 24V ride-on UTVs due to improper wiring that can cause overheating, smoking, and fires. The company has received 20 incident reports including five minor burns.
Product
Huffy Torex 24V Utility Terrain Vehicle (UTV) Ride-on toys
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25235·2025-04-24
Huffy 12-Volt Children's Ride-On Tonka Dump Trucks Fire Hazard
Huffy is recalling approximately 23,260 children's 12-volt ride-on Tonka Dump Trucks because the controller can overheat, posing fire and burn hazards. Consumers should stop using the trucks immediately and contact Huffy for a free replacement controller.
Product
Huffy 12-Volt Children's Ride-On Tonka Dump Trucks
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25238·2025-04-24
Kawasaki Motors 2025 KX motorcycles recalled for crash hazard
Kawasaki Motors is recalling about 3,400 model year 2025 KX series competition and cross-country motorcycles because the primary gear for the crankshaft can fail, creating a crash hazard. No injuries have been reported.
Product
Model Year 2025 KX series competition and cross-country motorcycles
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25234·2025-04-24
Roll Up Window Blinds Recalled for Strangulation and Entanglement Risk
BTAMREE roll up window blinds sold on Amazon.com are being recalled because their long operating cords pose a strangulation and entanglement hazard that can cause serious injury or death to children. Consumers should stop using the product immediately and contact BTAMREE for a refund.
Product
Roll Up Window Blinds
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25236·2025-04-24
Sondiko Butane Torches Recalled Due to Burn and Fire Hazards
Sondiko Butane Torches lack required child-resistant mechanisms and violate federal multipurpose lighter regulations, posing a risk of serious burn injuries or death to children. About 33,650 units were sold on Amazon from October 2023 through March 2025.
Product
Sondiko Butane Torches
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·25V276000·2025-04-24
International truck wiper linkage can separate causing wipers to fail
International is recalling certain 2025-2026 HV, HX, LT, MV, RH and 2025 EMV vehicles because the linkage connecting the right-side wiper arm to the motor may separate, causing the wipers to fail.
Product
INTERNATIONAL — INTERNATIONAL EMV, MV, LT, RH
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·25237·2025-04-24
Shape Sorter Car Toys Recalled Due to Choking Hazard
Deals Oasis recalls Kids Thrill Shape Sorter Car Toys because the included balls violate small-parts regulations for children under three and pose a choking hazard. No injuries have been reported.
Product
Kids Thrill Shape Sorter Car Toys
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·25233·2025-04-24
LuckupShein Window Roll Up Shades Recalled for Strangulation and Entanglement Hazards
About 545 LuckupShein window roll up shades sold on SHEIN.com have long operating cords that pose strangulation and entanglement hazards to children. The shades violate federal window covering regulations.
Product
LuckupShein Window Roll Up Shades
Category
Consumer Product
Distribution
Distributed nationwide

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