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 the agency’s own highest classification or reported deaths or serious injuries, 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

25901–25925 of 90145

SevereFDA (Drugs)·D-0765-2022·2022-04-20
FDA Recalls IDArubicin Injection for Particulate Matter Contamination
Teva Pharmaceuticals is recalling IDArubicin Hydrochloride Injection vials due to the presence of silica and iron oxide particulate matter. The recall affects nationwide distribution within the United States.
Product
IDArubicin Hydrochloride Injection USP 5gm/5mL (1mg/mL) for intravenous use, 5mL Single Dose Vial, Rx Only, Teva Pharmaceuticals, USA, Inc., North Wales, PA 19454, NDC 0703-4154-11.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0999-2022·2022-04-20
Giant Eagle Happy Face Cookies Recalled for Undeclared Milk Allergen
Giant Eagle recalled Happy Face Cookies from two Ohio stores due to undeclared milk allergen. Consumers with milk allergies should not consume these products.
Product
Giant Eagle, Happy Face Cookie Single 25065900000
Category
Food
Distribution
1 state
SevereNHTSA·22V268000·2022-04-20
Kibbi Recalls 2021 Renegade Motorhomes Due to Electrical Fire Risk
Kibbi, LLC is recalling 2021 Renegade Villagio and Vienna motorhomes because a stranded wire in the electrical relay may cause overheating and increase the risk of a fire.
Product
RENEGADE — RENEGADE VILLAGIO, VIENNA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0918-2022·2022-04-20
Cub 2 Enclosed Bed Canopy System Recalled Due to Potential Misuse
Sensory Medical Inc recalled 225 units of the Cub 2 Enclosed Bed Canopy System for potential misuse risk. The firm is updating product warnings and precautions for devices distributed before December 16, 2021.
Product
Cub 2 Enclosed Bed Canopy System
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1005-2022·2022-04-20
Back to Nature Cheese Crackers Recalled Due to Undeclared Egg and Milk Allergens
B&G Foods is recalling Back to Nature Cheddalicious Cheese Flavored Crackers due to undeclared egg and milk allergens caused by mispackaging. Consumers with egg or milk allergies should discard the product or return it.
Product
Back to Nature Cheddalicious Cheese Flavored Crackers 6 oz.. UPC: 8-19898-01491-0 6 cartons per case
Category
Food
Distribution
9 states
SevereFDA (Food)·F-0998-2022·2022-04-20
Giant Eagle Happy Face Cookies recalled for undeclared milk allergen
Giant Eagle is recalling Happy Face Cookie 4-packs due to undeclared milk allergen. Consumers with milk allergies should avoid this product.
Product
Giant Eagle, Happy Face Cookie 4 Pack 25051900000, 11 oz, Clam Shell
Category
Food
Distribution
1 state
HighFDA (Drugs)·D-0768-2022·2022-04-20
Clobetasol Propionate Lotion Recalled Due to Manufacturing Deviations
Preferred Pharmaceuticals is recalling Clobetasol Propionate Lotion 0.05% distributed in Illinois due to manufacturing deviations and discontinued stability study program. Consumers should contact their healthcare provider.
Product
Clobetasol Propionate Lotion 0.05%, Generic for Temovate, 118 mL bottle, Rx Only, Mfg: Teligent Pharma, Inc., PREFERRED Pharmaceuticals, Inc., The Physician's Solution, NDC 68788-7768-01
Category
Drug
Distribution
1 state
HighFDA (Devices)·Z-0916-2022·2022-04-20
ROTAWIRE guidewires recalled due to potentially compromised sterile pouch seals
Boston Scientific is recalling ROTAWIRE Drive guidewires due to potentially open pouch seals that could compromise product sterility. Affected units were distributed in the US, territories, Japan, and Canada.
Product
ROTAWIRE Drive and wireClip Torquer, ROTAWIRE Drive Extra Support
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0995-2022·2022-04-20
Skippy Reduced Fat Peanut Butter recalled for potential steel contamination
Skippy Reduced Fat Creamy Peanut Butter (40 oz) is being recalled due to potential steel contamination. No illnesses have been reported.
Product
SKIPPY Reduced Fat Creamy Peanut Butter NET WT 40 oz (2 LB 8 OZ) 1.13 kg UPC 037600105200 packaged in clear plastic jar with blue label.; SKIPPY Reduced Fat Creamy Peanut Butter NET WT 40 oz. (2 LB 8 OZ) 1.13 kg UPC 037600105200 packaged in clear plastic jar with blue label and…
Category
Food
Distribution
21 states
HighFDA (Devices)·Z-0922-2022·2022-04-20
FDA Recalls Abbott Vascular Priority Pack Accessory Kits for Leak and Connection Issues
Abbott Vascular is recalling 23 lots of Priority Pack accessory kits and packs due to reports of leaks and loose connections in the devices.
Product
20/30 Priority Pack Accessory Kit/.096 RHV - REF 1000186 WPL2122270-01 (2019-03-01) 20/30 Priority Pack w/.115 RHV - REF 1000186-115 WPL2122270-02 (2019-03-01)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0872-2022·2022-04-20
Conductivity Sensors in Dialog Hemodialysis Systems May Crack and Leak
B Braun Medical Inc is recalling conductivity sensors used in Dialog and Dialog+ hemodialysis systems due to potential cracks that could cause dialysate circuit leaks, affecting ultrafiltration during treatment.
Product
Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems. Conductivity Sensor (BIC) - VERSION 2, Article Code Number 3456102A. These conductivity sensors may be used as spare parts for the following dialysis machines: 710200L (UDI 04046963686345), 710200S (UDI…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0994-2022·2022-04-20
Wilton Cookie Bunny Hutch Kit Recalled for Missing Milk Allergen
Wilton Industries is recalling specific lots of Chocolate Cookie Bunny Hutch Kit because milk is not listed in the allergen statement, despite being present in the product.
Product
Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit, UPC: 0070896117274, total weight 28.7oz
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0940-2022·2022-04-20
CLARAVUE ECG Electrode May Fail to Deliver Effective Defibrillation
CLARAVUE Pre-wired ECG electrodes may not meet electrical safety standards for defibrillation, potentially delivering an ineffective electrical charge during emergency use. This is a Class II recall affecting devices nationwide.
Product
CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0873-2022·2022-04-20
Hemodialysis Conductivity Sensors recalled for potential cracks and dialysate leaks
B Braun Medical Inc is recalling conductivity sensors used in Dialog hemodialysis systems due to potential cracking during use, which could cause leaks in the dialysate circuit and improper ultrafiltration. Affected patients should contact their healthcare provider.
Product
Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems. Conductivity Sensor (END) - VERSION 2, Article Code Number 3456103A. These conductivity sensors may be used as spare parts for the following dialysis machines: 710200L (UDI 04046963686345), 710200S (UDI…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0931-2022·2022-04-20
Siemens Atellica CH Lithium reagent recalled for potential reagent carryover
Siemens Healthcare Diagnostics recalls approximately 2,158 units of Atellica CH Lithium_2 reagent (Lot Numbers 110108, 110185, 110238, 110302) due to potential for reagent carryover affecting quality control results, patient samples, and calibrator results.
Product
Atellica CH Lithium_2 (LITH_2), Siemens Material Number 11097637
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0928-2022·2022-04-20
Siemens Atellica CH Calcium_2 Reagent Carryover Recall
Siemens is recalling Atellica CH Calcium_2 diagnostic reagent due to potential reagent carryover that could impact quality control, patient samples, and calibrator results. The recall affects approximately 2,395 units distributed globally and in the US.
Product
Atellica CH Calcium_2 (CA_2), Siemens Material Number 11097644
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0903-2022·2022-04-20
Access-9 Hemostasis Valves Recalled for Guidewire Entrapment Risk
Merit Medical Systems is recalling 36,445 Access-9 Large Bore Hemostasis Valves due to an internal gap that can trap the guidewire, potentially delaying medical procedures.
Product
Access-9 Large Bore Hemostasis Valves, Catalog Code: 580775001, IN8112/C, K05-00053H, K05-00109G, K05-00137K, K05-00410G, K05-00438G, K05-00502F, K05-00587D, K05-01052, K05-01706C, K05-01880K, K05-02130, K05-02595, K09-12599A, K10-05487P, K12-00264, MAP111/F, MAP112/B, MAP112/F…
Category
Medical Device
Distribution
49 states
HighFDA (Food)·F-0983-2022·2022-04-20
Kroger Buttermilk Pancake & Waffle Mix Recalled for Foreign Material Contamination
Kroger Buttermilk Pancake & Waffle Mix with specific lot codes may contain foreign materials. Consumers who purchased this product should not use it.
Product
Item # 714-0706, Kroger Buttermilk Pancake & Waffle Mix. Product is shelf stable and packaged in a box. net wt. 2 lbs., UPC 0 11110 88219 6.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0934-2022·2022-04-20
Surgical Head Fixation Device Mount Clamp Assembly Deflection Recall
Deerfield Imaging recalls the Trumpf Mount Clamp Assembly component used in surgical head fixation devices. The clamp may deflect during use and become difficult to loosen after procedures, potentially requiring surgical intervention.
Product
Trumpf Mount Clamp Assembly (table adapter component), part #118704-000, a component of the IMRIS HFD100 head fixation device, models #119629-000 and #119630-000, which are used with ORT400 operating room tables.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0910-2022·2022-04-20
Orthopedic Surgical Instrument Kit Recalled for Improper Driver Fit
The Nextra Hammertoe Correction System surgical kit is being recalled due to an oversized driver that cannot properly connect to and remove from the implant. This defect can delay surgery.
Product
Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: NX-4532K Orthopedic surgical instrument
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0985-2022·2022-04-20
Krusteaz Buttermilk Pancake Mix Product Recalled Nationwide for Foreign Materials
Krusteaz Buttermilk Pancake Mix (Lot code KX2066, best-by 3/6/2024) is being recalled nationwide due to foreign materials. Consumers should not consume this product.
Product
Item # 721-0200, Krusteaz Buttermilk Pancake Mix. Product is shelf stable and packaged in a box. net wt. 2 lbs., UPC 0 41449 00110 4.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0915-2022·2022-04-20
Boston Scientific ROTAWIRE Drive guide wire devices recalled for open pouch seals
Boston Scientific is recalling ROTAWIRE Drive and ROTAWIRE Drive Floppy guide wire devices because pouch seals may be open, compromising sterility. The recall affects 433 5-packs distributed in the US, territories, Japan, and Canada.
Product
ROTAWIRE Drive and wireClip Torquer, ROTAWIRE Drive Floppy
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-0990-2022·2022-04-20
Gordon Choice Yellow Cake Mix nationwide recall for foreign materials
Continental Mills is recalling Gordon Choice Yellow Cake Mix (lot KX2066) nationwide due to the presence of foreign materials. The recall was voluntarily initiated on March 10, 2022.
Product
Item # 744-4875, Gordon Choice Yellow Cake Mix. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 93901 24575 5
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0935-2022·2022-04-20
ECG Electrode Set Fails Electrical Safety, May Prevent Effective Defibrillation
Graphic Controls' CLARAVUE pediatric electrode set fails electrical safety standards. The device may not deliver adequate charge during defibrillation, potentially rendering emergency treatment ineffective.
Product
CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776 50401-US
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0919-2022·2022-04-20
MUSE Cardiology System edits and diagnosis data lost after test signed
GE Healthcare's MUSE Cardiology Information System may lose test measurement edits and diagnosis statements after signing. The Class II recall affects 147 units in the US and internationally.
Product
MUSE Cardiology Information System, Model Numbers: a) 3101011-040, b) 3101010-401, c) 3101010-009, d) 3101010-008
Category
Medical Device
Distribution
0 states

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25901–25925 of 90145