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

20501–20525 of 27461

HighFDA (Devices)·Z-0212-2023·2022-11-23
CareFusion Genesis Sterile Containers Recalled for Failed Sterilization Validation Testing
CareFusion is recalling 308 units of Genesis sterilization containers that failed aerosol challenge testing required to ensure proper sterilization of surgical instruments. The containers were distributed in the US and multiple countries.
Product
CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD3-4ST
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0160-2023·2022-11-23
Similac Neosure Infant Formula Recalled Due to Compromised Seal Integrity
Abbott Laboratories is recalling Similac Neosure 2 fl oz bottles due to compromised seal integrity that could lead to spoilage. Approximately 14.5 million bottles distributed nationwide and internationally are affected.
Product
Similac Neosure 2 fl oz reclose able plastic bottle Packaged as: 48 count case
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0208-2023·2022-11-23
CareFusion GENESIS Sterilization Containers Fail Aerosol Validation Testing
CareFusion V.Mueller GENESIS sterilization containers have not consistently met aerosol challenge testing requirements. The recall affects 319 units distributed in the US and internationally.
Product
CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD2-4ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0242-2023·2022-11-23
Surgical Level 3 Gowns Recalled for Inadequate Fluid Protection
Texas Medical Technology Inc. is recalling 100,000 Disposable Surgical Level 3 Gowns (sizes Large, XLarge, XXLarge) because the fabric fails to pass hydrostatic pressure tests, meaning blood and other body fluids may penetrate the gown.
Product
Disposable Surgical Level 3 Gown, Size/Product Code: Large/GWS-03-L-B, XLarge/GWS-03-XL-B, XXLarge/GWS-03-XXL-B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0243-2023·2022-11-23
EasyStand Bantam standing devices may fail to maintain upright position
Altimate Medical is recalling EasyStand Bantam Small and Extra Small standers due to a component defect that may prevent the leg assembly bracket from maintaining the non-supine position. No injuries have been reported.
Product
EasyStand Bantam, with the following sizes. a. Small; b. Extra Small. Used for assisting individual in standing.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-0203-2023·2022-11-23
CareFusion Genesis Mini Sterilization Containers fail aerosol testing
CareFusion Genesis Mini Containers used for surgical instrument sterilization have not consistently met aerosol challenge testing requirements, which may affect their ability to protect instruments during sterilization.
Product
CareFusion V.Mueller GENESIS MINI CONTAINER 10-1/2 X 7-1/2" (26.7X19.0CM) 3" (7.6CM) DEEP STERRAD COMPATIBLE, REF CD0-3ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0241-2023·2022-11-23
GI4000 Electrosurgical Unit recalled due to power regulator failure risk
Steris recalls 5 GI4000 Electrosurgical Units with defective diode components that may cause power loss during endoscopic procedures.
Product
GI4000 Electrosurgical Unit - intended to deliver electrosurgical outputs to perform cutting and/or coagulation and coagulation with or without delivery of argon gas, in flexible endoscopic applications. MODEL #(s): G1110001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0227-2023·2022-11-23
Teleflex RUSCH Pocket Pac Urinary Catheter Kit Recalled for Sterility Concerns
Teleflex Medical recalled approximately 7,200 RUSCH Pocket Pac i.c. urinary catheter kits due to potential sterility issues. Patients should contact their healthcare provider and discontinue use.
Product
Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140 (IPN050116). Urinary catheter.
Category
Medical Device
Distribution
9 states
HighFDA (Food)·F-0153-2023·2022-11-23
Nash Family Creamery Ranch Cheese Curd recalled for undeclared soy
Nash Family Creamery Ranch Cheese Curd 8oz bags are recalled due to undeclared soy allergen. The product was distributed to Tennessee and Kentucky.
Product
Nash Family Creamery Ranch Cheese Curd packaged in 8oz plastic bag
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-0214-2023·2022-11-23
CareFusion Genesis Sterilization Containers Fail Aerosol Challenge Testing
CareFusion Genesis sterilization containers have failed to consistently meet aerosol challenge testing, potentially leaving surgical instruments inadequately sterilized. 318 units distributed in the US and internationally.
Product
CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD3-6ST
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0158-2023·2022-11-23
Similac Infant Formula Recalled Due to Compromised Seal Integrity
Abbott Laboratories is recalling Similac 360 Total Care Sensitive infant formula in 2 fl oz bottles due to compromised seal integrity that could lead to spoilage. Approximately 15.9 million bottles are affected across the United States and international locations.
Product
Similac 360 Total Care Sensitive 2 fl oz reclose able plastic bottle Packaged as: 6 count carton, 12 count carton, 48 count case
Category
Food
Distribution
1 state
HighNHTSA·22V874000·2022-11-23
2021-2022 Chevrolet Heavy-Duty Trucks Recalled for Suspension Lock Nut Defect
General Motors is recalling 2021-2022 Chevrolet 4500HD/5500HD/6500HD and XD models due to improperly heat-treated hex flange lock nuts in suspension and steering joints. The defective nuts may break, causing steering instability and increasing crash risk.
Product
CHEVROLET — 2022 CHEVROLET 4500XD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0218-2023·2022-11-23
CareFusion GENESIS Sterilization Containers Recalled for Inadequate Aerosol Challenge Testing
Carefusion 2200 Inc is recalling 562 Genesis STERRAD reusable sterilization containers due to failure to consistently meet aerosol challenge testing requirements, used to sterilize surgical instruments in healthcare facilities.
Product
CareFusion V.Mueller GENESIS LARGE, SHALLOW CONT. 28 X 11" (71.1 X 27.9CM) 3" (7.6CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD5-3ST
Category
Medical Device
Distribution
0 states
HighFDA (Drugs)·D-0067-2023·2022-11-23
Adam's Polishes Hand Sanitizer Recalled for Methanol Contamination
Adam's Polishes hand sanitizer with 75% isopropyl alcohol is being recalled due to methanol contamination found in certain lots manufactured under non-compliant conditions. The product was distributed nationwide.
Product
Adam's Polishes ALCOHOL BASED HAND SANITIZER, isopropyl alcohol 75% v/v, packaged in a) 4 fl. oz (118) spray bottle, NDC 74943-125-04; b) 8 fl. oz (237 mL) spray bottle, NDC 74943-125-08; c) 1 PINT / 16 fl. oz (475 ml.) spray bottle, NDC 74943-125-16; and d) 1 GALLON / 128 fl. oz
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0063-2023·2022-11-23
Carvedilol Tablets 25 mg Recalled for Weight and Thickness Specification Failures
Viatris Inc is recalling 2,794 bottles of Carvedilol Tablets 25 mg nationwide because the tablets exceed FDA specifications for weight and thickness. Patients should verify their lot number and contact their pharmacist if affected.
Product
Carvedilol Tablets, USP, 25 mg, 500-count bottles, Rx Only, Mfg: Mylan Pharmaceuticals Inc. Morgantown, WV 36505, Made in India, NDC 0378-3634-05
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0164-2023·2022-11-23
Similac Stage 1 infant formula recalled for seal integrity compromise
Abbott Laboratories is recalling Similac Stage 1 infant formula due to compromised seal integrity that could lead to product spoilage. Affected batches were distributed across the U.S., Canada, and Latin America.
Product
Similac Stage 1 (Export Dominican Republic) 2 fl oz reclose able plastic bottle Packaged as: 48 count case
Category
Food
Distribution
1 state
HighFDA (Food)·F-0150-2023·2022-11-23
Gem City Fine Foods Flourless Chocolate Torte Recalled for Undeclared Soy
Gem City Fine Foods is recalling its GF Flourless Chocolate Torte due to mislabeling. The product was labeled as Triple Berry Streusel Cheesecake, leaving soy undeclared on the package.
Product
Gem City Fine Foods GF Flourless Chocolate Torte, 4 oz., frozen gluten free dessert, clear plastic package, UPC 855026001018, Gem City Fine Foods, LLC, 3403 S 1400 W, Suite C, W Valley City, UT 84119
Category
Food
Distribution
1 state
HighFDA (Drugs)·D-0060-2023·2022-11-23
ImprimisRx Timolol-Latanoprost Ophthalmic Drops Recalled for Subpotent Active Ingredient
ImprimisRx is recalling 960 bottles of compounded Timolol-Latanoprost ophthalmic drops nationwide. Affected batches contain less than 90% of the labeled latanoprost amount.
Product
Timolol-Latanoprost (0.5/0.005%) ophthalmic drops, Compounded, 5 mL bottle, Imprimis Rx, Ledgewood, NJ.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0062-2023·2022-11-23
Injectable Sodium Chloride Recalled for Potential Container Leaks Compromising Sterility
ICU Medical is recalling 137,120 bags of 0.9% Sodium Chloride Injection because bags may leak and potentially compromise sterility. The affected lot (5829936) was distributed nationwide.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0163-2023·2022-11-23
Abbott Similac Stage 1 infant formula recalled for compromised seal integrity
Abbott Laboratories is recalling Similac Stage 1 infant formula due to compromised seal integrity on 14,588,544 bottles. The defect could allow product spoilage.
Product
Similac Stage 1 (Export Colombia) 2 fl oz reclose able plastic bottle Packaged as: 48 count case
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0230-2023·2022-11-23
Spinal Decompression System Recalled for Potential Weld Breakage
Boston Scientific is recalling 175 Superion Indirect Decompression System devices due to potential weld breakage at the spindle cap that may prevent proper deployment during implantation.
Product
Superion¿ Indirect Decompression System (IDS) Model Numbers and Size: 101-9808 - 8mm 01-9812 - 12mm 101-9814 - 14mm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0206-2023·2022-11-23
CareFusion GENESIS Sterilization Containers Fail Aerosol Challenge Testing
CareFusion GENESIS sterilization containers have not consistently met aerosol challenge testing requirements. Approximately 1,132 units distributed to healthcare facilities in the U.S. and internationally are affected.
Product
CareFusion V.Mueller GENESIS HALF-LENGTH CONTAINER 11X12" (27.9 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE, REF CD1-5ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0210-2023·2022-11-23
CareFusion Genesis sterilization containers recalled for failed sterility testing
CareFusion Genesis reusable sterilization containers are recalled after failing aerosol challenge testing requirements. No illnesses or injuries have been reported.
Product
CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD2-6ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0211-2023·2022-11-23
CareFusion sterile containers fail aerosol sterilization test requirement
CareFusion GENESIS sterilization containers did not consistently meet aerosol challenge testing requirements. These containers are used in healthcare facilities to sterilize surgical instruments.
Product
CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 8" (20.3CM) DEEP STERRAD COMPATIBLE, REF CD2-8ST
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0215-2023·2022-11-23
GENESIS Full-Length Sterilization Containers recalled for failed aerosol testing
CareFusion 2200 Inc recalls GENESIS sterilization containers (model CD3-7ST, all lots) that have not consistently met aerosol challenge testing requirements required for proper sterilization efficacy.
Product
CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 7" (17.8CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD3-7ST
Category
Medical Device
Distribution
0 states

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20501–20525 of 27461