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

11751–11775 of 27718

HighFDA (Devices)·Z-2352-2024·2024-07-24
Medtronic Ascenda Intrathecal Catheter design update to prevent occlusion
Medtronic is updating the design of its Ascenda Intrathecal Catheter (Models 8780, 8781, 8784) to reduce potential tissue growth into the catheter connector that may cause occlusion. Approximately 111,762 units were distributed worldwide.
Product
Medtronic Ascenda Intrathecal Catheter, Models: a) 8780 (114 cm); b) 8781 (140 cm); c) 8784 (catheter pump revision kit)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2353-2024·2024-07-24
Qiagen QIAcube Connect MDx heating failure may cause erroneous diagnostic results
A heating defect in the Qiagen QIAcube Connect MDx may prevent proper incubation temperatures below 40°C, potentially affecting diagnostic test results.
Product
QIAcube Connect MDx - IVD Instrument designed to perform automated isolation and purification of nucleic acids in molecular diagnostic and/or molecular biology applications. Model/Catalog Number: 900370 Software Version: 1.0.1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1495-2024·2024-07-24
Black coffee canned beverages recalled nationwide for potential under-processing
Snapchill, LLC is recalling 549,146 cans of black coffee beverages nationwide and in Canada due to potential under-processing. Affected cans have expiration dates between June 16, 2024 and April 16, 2025.
Product
Black Coffee Canned Beverage packaged under the following brands and sizes: 1. 41 & Change Coffee Co A Finca / Nicaragua Cold Coffee, 12 oz. UPC 1 97644-95863 4. 2. Alchemy Roast Elixir or Life (Gutemala/Huehuetenango Blend) 12 oz. UPC 8 10149-37056 4. 3. Amavida Coffe Roa
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2388-2024·2024-07-24
Infusion pump IV administration set recalled for backcheck valve malfunction risk
B. Braun is recalling Infusomat UNIV. 15 DROP PUMP SET infusion sets due to potential backcheck valve malfunction that may cause medication to flow backward into primary IV containers and prevent proper priming, risking adverse drug reactions.
Product
Infusomat UNIV. 15 DROP PUMP SET, 2 CARESITE, ASV-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication Model/Catalog Number: 363421
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2358-2024·2024-07-24
Abbott Proclaim XR 5 Implantable Pulse Generator Battery Labeling Error
Abbott Proclaim XR 5 implantable pulse generators may reach end of service sooner than product labeling indicates, affecting approximately 83,511 units worldwide. Patients should contact their healthcare provider for guidance on device monitoring and replacement planning.
Product
Abbott Proclaim XR 5 Implantable Pulse Generator, REF 3660, Sterile EO, Rx Only
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2354-2024·2024-07-24
Knee Walker Tiller Separation Risk Recalled Due to Fall Hazard
Medical Depot is recalling Nitro Glide Knee Walker Model 791BL units due to a defect where the tiller may separate from the base assembly. If the device fails, users may fall and sustain injury.
Product
Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury the ability to remain mobile and glide through their daily activities. Model: 791BL (Blue)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2405-2024·2024-07-24
Zimmer Tourniquet Cuff Recalled Due to Incorrect Port Configuration Labeling
Stryker is recalling 90 units of Zimmer Tourniquet Cuff 30" because packaging labels them as dual port single bladder, but they actually contain a single port single bladder configuration.
Product
REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2408-2024·2024-07-24
High Flow Insufflation Tubing Recalled for Incomplete Seals
Canadian Hospital Specialties is recalling HIGH FLOW INSUFFLATION TUBING with incomplete seals that may result in non-sterile product. The defect affects 6,300 units and poses patient safety concerns.
Product
Product Name: HIGH FLOW INSUFFLATION TUBING (with Filter) Model/Catalog Number: 20400161S Product Description: Laparoscopic Insufflator
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·24307·2024-07-18
CFMOTO ZFORCE 950 ROVs Recalled for Crash and Tip-Over Hazards
CFMOTO is recalling approximately 3,630 ZFORCE 950 HO Sport Side-by-Side recreational off-highway vehicles from 2022–2023 because the shock absorber rod assembly can unthread and detach, causing suspension collapse and crash or tip-over hazards.
Product
CFMOTO ZFORCE 950 HO Sport Side-by-Side ROVs (2022-2023)
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·24308·2024-07-18
Manhattan Toy Brilliant Bee Rattles Recalled for Choking Hazard
Sassy Baby Inc. is recalling about 3,000 Manhattan Toy Brilliant Bee Rattles because the wooden base can detach and release plastic rings that pose a choking hazard to young children.
Product
Brilliant Bee Rattles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24309·2024-07-18
BISSELL Steam Shot Handheld Steam Cleaners Recalled for Burn Hazard
BISSELL is recalling about 3.2 million Steam Shot Handheld Steam Cleaners because they can expel hot water or steam during heating or use, causing burn injuries. The company has received 183 reports of hot water or steam escaping, including 157 reports of minor burn injuries.
Product
BISSELL® Steam Shot™ Handheld Steam Cleaners
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2252-2024·2024-07-17
Medical Device Recall: Bausch+Lomb Intravitreal Injection Kit Unvalidated Sterilization
Synergetics Inc is recalling Bausch+Lomb I-PACK Intravitreal Injection Kits because sterilization certificates could not be validated by the supplier. The FDA classified this as Class I.
Product
BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye)
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1464-2024·2024-07-17
Crecelac Infant Powdered Formula Recalled Due to Cronobacter
Dairy Manufacturers' Crecelac Infant formula (5,376 cans distributed in Texas) is recalled due to Cronobacter spp. detected during FDA testing. Products lack required premarket evaluation for food safety and nutritional standards.
Product
Crecelac Infant 0-12 powdered infant formula with iron 12.4 oz cans
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-2254-2024·2024-07-17
Intravitreal Injection Kit Recalled for Unvalidated Sterilization Certificates
Synergetics Inc is recalling 35 units of the BAUSCH+LOMB I-PACK Intravitreal Injection Kit because sterilization certificates could not be validated, creating an infection risk.
Product
BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eye)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0588-2024·2024-07-17
OTC Sunscreen Foundation Recalled for Fungal Mold Contamination
Suntegrity IMPECCABLE SKIN sunscreen foundation is recalled for microbial contamination with Aspergillus Sydowii mold. Consumers should discontinue use immediately.
Product
IMPECCABLE SKIN - IVORY — IMPECCABLE SKIN - IVORY (ZINC OXIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2315-2024·2024-07-17
Baxter iLED 7 surgical lights recalled due to thermal burn risk
Baxter Healthcare is recalling iLED 7 surgical lights due to customer reports of thermal skin injuries. The recall affects approximately 6,243 units distributed worldwide.
Product
iLED 7 surgical lights, Model Numbers: a) 4068110 (Ceiling Single Surgical Light); b) 4068120 (Mobile Surgical Light); c) 4068140 (Pendant Surgical Light); d) 4068210 (Ceiling Duo Surgical Lights); e) 4068310 (Ceiling Trio Surgical Lights); f) 4068410 (Ceiling Quad
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-1468-2024·2024-07-17
7-Eleven Simply Egg Salad Sandwich recalled due to undeclared milk allergen
Taylor Farms Northwest LLC has voluntarily recalled 7-Eleven Simply Egg Salad Sandwich (6.8 oz) due to undeclared milk, affecting products distributed in Oregon and Washington.
Product
7-Eleven Simply Egg Salad Sandwich, Keep Refrigerated, Flexible Packaging, 6.8oz (193g)
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-2314-2024·2024-07-17
Baxter Trulight Surgical Lights Recalled for Thermal Skin Injuries
Baxter Healthcare Corporation recalled Trulight 5000/3000 Surgical Light systems due to customer reports of thermal skin injuries. The urgent medical device correction affects models 4038210 and 4038310 distributed worldwide.
Product
Trulight 5000/3000 Surgical Light, model numbers: a) 4038210 (Duo Surgical Lights}; b) 4038310 (Trio/Quad Surgical Lights)
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-1472-2024·2024-07-17
Arepas La Mejor Arepa de Chocolo Recalled for Undeclared Milk Allergen
Villa Nueva Interservices is recalling Arepas La Mejor Arepa de Chocolo due to undeclared milk allergen. Consumers with milk allergies are at risk.
Product
Arepas La Mejor, Arepa de Chocolo (Chocolate Sweet Corn Pancakes), NET WT. 25 Oz., 5 units per package, KEEP REFRIGERATED
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-2251-2024·2024-07-17
Bausch+Lomb I-PACK Injection Kit Recalled for Unvalidated Sterilization
Synergetics Inc is recalling the Bausch+Lomb I-PACK Injection Kit nationwide because sterilization certificates could not be validated by the supplier. The unvalidated sterilization of this eye injection device poses a potential infection risk.
Product
BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2253-2024·2024-07-17
BAUSCH+LOMB I-PACK Injection Kit Recalled Due to Sterilization Validation Failure
FDA has recalled 116 units of BAUSCH+LOMB I-PACK Injection Kits because sterilization certificates could not be validated by the supplier, creating potential infection risk for patients receiving intravitreal eye injections.
Product
BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1463-2024·2024-07-17
Powdered infant formula recalled for missing safety evaluation
Farmalac powdered infant formula was recalled because the manufacturer failed to submit required premarket notification to the FDA. The product was never evaluated for safety or nutritional standards.
Product
Farmalac powdered infant formula with iron 12.4 oz cans
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-2313-2024·2024-07-17
Baxter VidiaPort and Trulight surgical lights recalled for thermal burn risk
Baxter Healthcare Corporation is recalling VidiaPort and Trulight surgical light systems due to customer reports of thermal skin injuries. Approximately 275 units were distributed worldwide.
Product
VidiaPort carrying arm, mount for auxiliary products, model numbers: a) 4028110 (Ceiling Single Surgical Light); b) 4028210 (Ceiling Duo Surgical Lights); c) 4028310 (Ceiling Trio Surgical Lights)
Category
Medical Device
Distribution
0 states
SevereFDA (Food)·F-1466-2024·2024-07-17
Queso Rico La Hacienda Queso Fresco Cheese Recalled for Listeria
Queso Rico La Hacienda brand queso fresco cheese was found to contain Listeria monocytogenes. FDA Class I recall affects 640 pounds distributed to retail stores in Texas counties.
Product
Queso Rico La Hacienda brand queso fresco cheese packaged in 9 oz, 1 pound, and 2 pound plastic packages. Product labeling reads in part "***QUESO RICO LA HACIENDA***EL QUESO FRESCO FRESCO DE VERACRUZ***Lic. Permit #483709 El Queso Rico "LA HACIENDA"***5617 E. Trenton Rd., Suite
Category
Food
Distribution
0 states
SevereFDA (Food)·F-1465-2024·2024-07-17
Infant Formula Recalled for Lack of Premarket Safety Evaluation
Farmalac 0-12 Low lactose powdered infant formula is being recalled because the manufacturer did not submit required premarket notification to the FDA. The product has not been evaluated against U.S. food safety and nutritional standards.
Product
Farmalac 0-12 Low lactose powdered infant formula with iron 12.4 oz cans
Category
Food
Distribution
0 states

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11751–11775 of 27718