Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

11351–11375 of 13816

ModerateFDA (Devices)·Z-1619-2022·2022-08-31
McKesson Medefil Normal Saline IV Flush Syringes Recalled for Temperature Exposure
McKesson is recalling Medefil Normal Saline IV Flush Syringes (Models MIS-1130 and 191-MIS-1130) due to facility temperature excursions between June and August 2021. Products received through September 30, 2021 may have impaired effectiveness from temperature exposure prior to delivery.
Product
a. Medefil Normal Saline IV Flush Syringe NORMAL SALINE FLUSH, SYR 10ML/12ML (60/BX 16BX/CS), Model Number: MIS-1130. b. MEDEFIL INC McKesson SALINE IV FLUSH, SYR NORMAL 10ML/12ML .9% (60/BX 16BX/CS) Model Number: 191-MIS-1130.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1611-2022·2022-08-31
IV Securement Kit Recall Due to Storage Temperature Damage
McKesson is recalling Medline Centurion IV Securement Kits that were exposed to high temperatures during storage, which may have impacted product effectiveness. No illnesses have been reported.
Product
MEDLINE INDUSTRIES Centurion IV Securement Kit Model Number: IVSSTK3
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1624-2022·2022-08-31
Fisher Scientific Sure-Vue Pipette Recall Due to Temperature Exposure
Mckesson Medical-Surgical is recalling Fisher Scientific Sure-Vue RPR Dispensing Pipettes due to temperature excursions during storage from June to August 2021. Exposure to higher temperatures may have impacted product effectiveness.
Product
FISHER SCIENTIFIC Sure-Vue PIPETTE, RPR DISPENSING (500/PK) Catalog # 23038015
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1589-2022·2022-08-31
Drugs of Abuse Test Kits Recalled Due to Temperature Exposure
McKesson Medical-Surgical is recalling multiple brands of drugs of abuse test kits because temperature excursions prior to delivery may have reduced product effectiveness.
Product
Drugs of Abuse Tests: a. Wondfo Tdip Drugs of Abuse Test Tdip Single Drug Fentanyl (FEN) Urine Sample 25 Tests. Model Number: AWFTY-114. b. Alere Drugs of Abuse Test E-Z Split Key Cup 12-Drug Panel AMP, BAR, BUP, BZO, COC, mAMP/MET, MDMA, MOP, MTD, OXY, PPX, THC Urine S
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1622-2022·2022-08-31
Dynarex Nail Polish Remover Pads Recalled for Reduced Effectiveness from Heat Exposure
Mckesson Medical-Surgical Inc. is recalling Dynarex Nail Polish Remover Pads due to facility temperature excursions in summer 2021 that may have reduced product effectiveness. All lots received between June 1 and September 30, 2021, nationwide are affected.
Product
Dynarex¿ PAD, NAIL POLISH REMOVER (100/BX 10BX/CS) DYNREX Catalog # 1501
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1596-2022·2022-08-31
FDA Recalls Heparin Sodium Prefilled Syringes Due to Heat Damage
Mckesson Medical-Surgical Inc. is recalling Excelsior Heparin Sodium prefilled syringes that may have been damaged by temperature excursions during manufacturing, potentially affecting their effectiveness. The recall covers lots received between June and September 2021.
Product
Excelsior Heparin Sodium, Porcine, Preservative Free 100 U / mL Solution Prefilled Syringe, Partial Fill 5 mL Fill in 10 mL Syringe Model Number: 513604
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1569-2022·2022-08-31
Anatomical Model Recalled for Wrong Product Shipped in Packaging
Materialise USA LLC is recalling ProPlan CMF Anatomical Model units where packages labeled MU22-INA-DUQ contained the wrong anatomical model inside. Recipients should verify their package contents match the label.
Product
ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1512-2022·2022-08-24
HeartWare HVAD System Batteries Recalled for Critical Electrical Faults
HeartWare HVAD System Batteries are being recalled due to electrical faults that may prevent the battery from powering the device controller, accepting charges, or maintaining charge. Approximately 19,616 batteries distributed worldwide are affected.
Product
HeartWare Ventricular Assist Device (HVAD) System Batteries, Product Number 1650DE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1531-2022·2022-08-24
Contact Lens Multi-Purpose Solution Recalled for Improper Storage
Family Dollar is recalling BIOTRU Multi-Purpose Solution (4 oz, SKU 999009) due to improper temperature-controlled storage. Approximately 1,051 units were affected across US Family Dollar stores.
Product
B L BIOTRU MULTI PURPOSE SOLUTION 4 FLOZ, SKU 999009
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1554-2022·2022-08-24
Surgical forceps recalled due to potentially compromised sterile barrier
Stradis Medical recalls 850 surgical forceps (NARMD MEDICAL DEPOT Forceps, part ZZ-0701) due to potentially compromised sterile barriers. Healthcare facilities with these units should identify affected lot numbers and contact the manufacturer for guidance.
Product
NARMD MEDICAL DEPOT Forceps - Kelly Curved 5.5"; Part Number: ZZ-0701
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1550-2022·2022-08-24
Dressing Change Kit Mislabeled as Latex-Free Contains Natural Rubber Latex
Trinity Sterile's Wolf Pak Premium Dressing Change Kit is mislabeled as latex-free but contains natural rubber latex in component 94-7002. This poses a risk to people with latex allergies.
Product
Wolf Pak Premium Dressing Change Kit with Statlock CS/30 Ref: DC5040LF
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1528-2022·2022-08-24
Veriquick Pregnancy Test 2CT Recalled for Improper Storage
Family Dollar is recalling Veriquick Pregnancy Test 2CT kits (SKU 903756) sold from May 1 to June 10, 2022 due to improper storage outside temperature-controlled areas.
Product
Veriquick Pregnancy Test 2CT, SKU 903756
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1553-2022·2022-08-24
Surgical forceps recalled due to compromised sterile barrier
Stradis Medical is recalling NARMD MEDICAL DEPOT Kelly Straight forceps because the sterile barrier may be compromised. The recall affects 825 units distributed nationwide in South Carolina.
Product
NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5"; Part Number: ZZ-0700
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1555-2022·2022-08-24
BD PhaSeal Y-Site Connector recalled for mislabeled expiration dates
Becton Dickinson recalls 9,340 units of BD PhaSeal Y-Site Connectors (Catalog 515304) due to incorrect expiration dates printed on product labels that extend beyond the actual product expiration.
Product
BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanically prohibits the transfer of environmental contaminants into the system and the escape of drug or vapor concentrations outside the system. Catalog Number: 51530
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1541-2022·2022-08-24
Skin liquid bandage recalled for improper temperature storage
Family Dollar's NEW SKIN Liquid Bandage was not stored in temperature-controlled conditions, potentially compromising product integrity. Affected units were sold nationwide during May through June 2022.
Product
NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ, SKU 999417
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1526-2022·2022-08-24
Pregnancy Test Units Recalled Due to Improper Temperature Storage
Clearblue Smart Countdown pregnancy tests distributed to Family Dollar stores were not stored in temperature-controlled conditions. Consumers who purchased this product should return it for a refund or replacement.
Product
CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT, SKU-ID 900260
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1556-2022·2022-08-24
FDA Recalls Echelon-14 Microcatheters Due to Moisture-Exposed Packaging
Micro Therapeutics is recalling Echelon-14 microcatheters whose outer carton packaging was exposed to a wet substance during transport, posing a risk to device sterility.
Product
Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1518-2022·2022-08-24
Abbott Alinity m Diagnostic System Recalled for Incorrect Optical Calibration
Abbott Molecular is recalling the Alinity m System due to incorrect optical calibration. The affected unit (Serial Number 00654) was distributed to Italy.
Product
The Alinity m System, REF 08N53-002, For In Vitro Diagnostic Use.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1532-2022·2022-08-24
CURAD First Aid Kit Recalls Due to Improper Storage Temperature
Family Dollar is recalling CURAD First Aid Kits (SKU 999037) that were improperly stored without temperature control from April 30 to June 10, 2022. The temperature exposure may have degraded medications or compromised medical devices within the kits.
Product
CURAD FIRST AID KIT, SKU 999037
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1538-2022·2022-08-24
Fixodent denture adhesive cream recalled for improper storage
Family Dollar is recalling Fixodent Org Cream denture adhesive (2.4oz and 0.75oz travel sizes) sold May-June 2022 due to improper storage in non-temperature-controlled areas. No illnesses reported.
Product
FIXODENT ORG CREAM 2.4OZ, SKU 906018 FIXODENT ORG CREAM TRAVEL .75OZ, SKU 901239
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1530-2022·2022-08-24
SKYN Non-Latex Condoms Recalled Due to Improper Storage
Family Dollar is recalling SKYN Original, Elite, and LS non-latex condoms due to improper storage. Products sold between May 1 and June 10, 2022 were not stored in temperature-controlled conditions.
Product
SKYN ORIGINAL NON LATEX CONDOM 12CT, SKU 903409 LS SKYN NON LATEX LUBRICATED CONDOM 3CT, SKU 900794 SKYN ELITE NON LATEX CONDOM 12CT, SKU 903415
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1557-2022·2022-08-24
Echelon-14 Micro Catheter Recall Due to Moisture Exposure During Transport
Micro Therapeutics is recalling Echelon-14 Micro Catheters because outer packaging was exposed to moisture during transport. The moisture exposure could compromise the sterility or function of the device.
Product
Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1548-2022·2022-08-24
Medical dressing tray mislabeled as latex-free but contains natural rubber latex
Trinity Sterile's IV catheter dressing trays are mislabeled as latex-free despite containing natural rubber latex in component 94-7002, risking allergic reactions in latex-sensitive users.
Product
Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1552-2022·2022-08-24
FDA Recalls Stradis Medical Surgical Scissors Due to Compromised Sterile Barrier
Stradis Medical is recalling NARMD MEDICAL DEPOT Iris Curved Scissors (Part Number ZZ-0697) because the sterile barrier may be compromised, potentially exposing patients to contamination during surgical procedures.
Product
NARMD MEDICAL DEPOT Scissors Iris Curved 4.5", Part Number ZZ-0697
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1543-2022·2022-08-24
GS Saline Solution recalled due to improper temperature storage
GS Saline Solution (12 fl oz) was not stored in temperature-controlled areas, risking contamination. The affected product was sold at Family Dollar stores nationwide from May 1–June 10, 2022.
Product
GS SALINE SOLUTION 12FL OZ, SKU 902274
Category
Medical Device
Distribution
Distributed nationwide

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11351–11375 of 13816