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

25826–25850 of 90145

SevereFDA (Food)·F-1004-2022·2022-04-27
Carol's Cuts Fresh-Cut Cantaloupe Fruit Medley Recalled for Salmonella
Carol's Cuts Fruit Medley is recalled due to fresh-cut cantaloupe testing positive for Salmonella. The affected product was distributed to retail, military, food service, and schools in Kansas, Missouri, Iowa, and Nebraska.
Product
Carol's Cuts Fruit Medley Ingredients may include Honey, cantaloupe, pine, and grape Prepared: Carols Cuts 1247 Argentine Blvd, KC KS 66105 Net Weight 8oz, Net Weight 16oz UPC: 852193001087, 852193900458 Best If Used By: 03/21/22, 03/23/22, 03/27/22, 03/26/22, 03/24/22 Product…
Category
Food
Distribution
4 states
SevereFDA (Food)·F-1006-2022·2022-04-27
WFM 365 Organic Creamy Caesar Dressing Recalled for Undeclared Wheat and Soy
Whole Foods Market is recalling WFM 365 Organic Creamy Caesar dressing due to undeclared wheat and soy allergens. Consumers with allergies to these ingredients should not consume the product.
Product
WFM 365 Organic Creamy Caesar, 12oz, UPC#99482490290, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods Market Austin, TX
Category
Food
Distribution
3 states
SevereFDA (Drugs)·D-0782-2022·2022-04-27
artnaturals Hand Sanitizer Recalled for Benzene and Chemical Contamination
artnaturals ethyl alcohol hand sanitizer (8 fl oz bottles, lot G20127E and G20128A, exp. 5/1/2022) is recalled nationwide due to chemical contamination including benzene, acetaldehyde, and acetal.
Product
artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA 90248, UPC: 8 16820 02820 5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1008-2022·2022-04-27
Super Twa Mushroom Mixed Mushrooms Recalled Due to Listeria Monocytogenes
Farm Fresh Produce LLC is recalling Super Twa Mushroom Mixed Mushrooms (14.11 oz) due to Listeria monocytogenes contamination identified in California. The recall affects 160 cases distributed in California only.
Product
Super Twa Mushroom Mixed Mushrooms; New Wt/When Packed) 14.11 oz. (400g) Keep refrigerated. UPC: 6957937481850
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-0785-2022·2022-04-27
FDA Recalls Pink Pussycat Sensual Enhancement Capsules for Undeclared Sildenafil
Pink Pussycat Sensual Enhancement capsules are being recalled nationwide. The FDA found they contain undeclared sildenafil and were marketed without FDA approval.
Product
Pink Pussycat SENSUAL ENHANCEMENT capsule, 3000mg, 1-count blister card, Manufactured for: Pink Pussycat Products - Chatsworth, CA 91311, UPC 8 91875 00462 6.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0907-2022·2022-04-27
Philips Respironics V60 Ventilator Recalled Due to Electrical Circuit Defect
Philips Respironics V60 ventilators are recalled due to an internal electrical circuit defect that may cause the device to stop operating. Approximately 87,138 units worldwide are affected.
Product
Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 1053617, 1053618, 1076709, 1076716, 1076717, 1137292, DU1053617, U1053617, R1053618, R1076709)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0908-2022·2022-04-27
Philips Respironics V60 Plus Ventilator Recalled for Electrical Circuit Failure Risk
Philips Respironics V60 Plus Ventilators are recalled for an internal electrical circuit defect that could cause the device to stop operating. Approximately 12,145 units were affected worldwide.
Product
Philips Respironics V60 Plus Ventilator (All Models, including: 1138747, 1137276)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0909-2022·2022-04-27
Philips Respironics V680 Ventilator May Stop Operating Due to Electrical Fault
Philips Respironics V680 Ventilators may stop operating due to an internal electrical circuit fault. Units were distributed worldwide and across the United States.
Product
Philips Respironics V680 Ventilator (All Models, including: P/N 1103044 (850011)), *Distributed outside the United States
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0927-2022·2022-04-27
Medtronic Harmony Delivery Catheter System Recalled Over Equipment Failure Risk
Medtronic is recalling 1,483 Harmony Delivery Catheter Systems due to potential capsule bond failure during pulmonary valve replacement procedures. The FDA has classified this as a Class I recall affecting devices distributed in the US and Canada.
Product
Harmony Delivery Catheter System. Part of the Harmony Transcatheter Pulmonary Valve (TPV) Replacement Implantation System.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1009-2022·2022-04-27
Enoki Mushrooms Recalled Due to Listeria Monocytogenes Contamination
Wisetrade Corporation is recalling Global Fresh Marketing Enoki Mushrooms because the California Department of Public Health detected Listeria monocytogenes contamination during product sampling. Consumers should not consume the product.
Product
Global Fresh Marketing Enoki Mushrooms Champignons d'Enoki Net Wt/Poids 200g/7.05 oz. Vacuumed Plastic bag UPC: 809728-95012 Wisetrade Corporation, Irvine, CA 92618
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0946-2022·2022-04-27
Virus Counter Platform VC3100 Class II Medical Device Recall
Sartorius Corporation is recalling the Virus Counter Platform Model VC3100 (model numbers VIR-92166, VIR-92341) distributed nationwide to 82 units, classified as a Class II FDA medical device recall.
Product
Virus Counter Platform with Model Name VC3100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0951-2022·2022-04-27
Genetic Testing Kit Recalled for Inaccurate Mutation Test Results
Qiagen Sciences' KRAS mutation testing kit can produce false positive or false negative results due to testing flags or warnings. 435 kits distributed across 16 U.S. states are affected.
Product
therascreen KRAS RGQ PCR Kit (24) Model Number(s): REF 870021 (US IVD)
Category
Medical Device
Distribution
17 states
HighFDA (Food)·F-1011-2022·2022-04-27
Miller's Ale House Ice Cream Recalled for Undeclared Allergens
Specialty Desserts Services is recalling Miller's Ale House Capt. Jack's Buried Treasure ice cream due to failure to declare milk, egg, wheat, soy, almonds, and coconut allergens. Consumers with these allergies should not consume the product.
Product
MILLER'S ALE HOUSE, CAPT. JACK'S BURIED TREASURE, Vanilla Ice Cream, Oreo, Heath Bar, Caramel and Hot Fudge. AYE CAPTAIN!
Category
Food
Distribution
0 states
HighFDA (Devices)·Z-0972-2022·2022-04-27
X-ray Imaging System May Fail to Cool Tube Properly
Siemens Artis zee biplane MN X-ray systems may have inadequate cooling in the X-ray tube circuit, causing automatic system shutdown during operation. Seven affected systems are distributed nationwide.
Product
Artis zee biplane MN, Model Number 10094143
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0947-2022·2022-04-27
Matrix COVID-19 Test Kits Recalled for Unauthorized Home Sample Collection
Matrix Medical Network is recalling 3,226 At-Home COVID-19 Test kits distributed across 24 U.S. states because the tests were not authorized by the FDA for home sample collection.
Product
Matrix Clinical Solution At-Home COVID-19 Test
Category
Medical Device
Distribution
25 states
HighFDA (Devices)·Z-0962-2022·2022-04-27
CT Scanner Software Error May Cause Scanning Interruptions and Unexpected Radiation
Siemens SOMATOM CT scanners with software syngo CT VA30A_SP4 may experience sporadic software errors causing scanning interruptions and potential unexpected radiation doses. 547 units affected nationwide.
Product
SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now 11061610 & 11061618 SOMATOM go.Up 11061620 & 11061628 SOMATOM go.All 11061630 & 11061638 SOMATOM go.Top 11061640 & 11061648 SOMATOM go.Sim 11061660 & 11061668 SOMATOM go.Open Pro 11061670…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0781-2022·2022-04-27
Sermorelin Acetate Injection Recalled Due to Sterility Assurance Issues
Sermorelin Acetate injectable (76 vials) recalled nationwide due to manufacturing deviations that compromise sterility assurance. No illnesses reported.
Product
Sermorelin Acetate 1 mg/mL (6 mL) Injection, 6 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0958-2022·2022-04-27
Acumed Cannulated Screws May Lack Sufficient Strength for Bone Fixation
Acumed 4.0mm x 10mm Cannulated Screws may not have sufficient strength to hold bone fragments in place. This could result in improper bone healing, fracture, or soft tissue damage.
Product
4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0965-2022·2022-04-27
Cardiac Device Programmer Software May Fail to Terminate Test
St. Jude Medical's Merlin 2 programmer software can fail to stop a clinical Decrement Test and restore pacing parameters during in-clinic testing, affecting 401 devices worldwide.
Product
Merlin 2 PCS MER3700 programmer Model MER3400 software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0950-2022·2022-04-27
FDA recalls Regard IV Start Kit component over safety issue
Resource Optimization & Innovation LLC is recalling 3,570 Regard IV Start Kits due to a recalled component, the PDI Prevantics Swab. The affected kits were distributed to two consignees in Missouri.
Product
Regard IV Start Kit for preparing and/or dressing a peripheral vein intravenous access site
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-0988-2022·2022-04-27
Gallant DR Implantable Cardioverter Defibrillator Bluetooth Malfunction Affects Remote Monitoring
St. Jude Medical's Gallant DR implantable cardioverter defibrillator has a Bluetooth malfunction preventing remote monitoring and reducing battery life. The device enters inductive-only telemetry mode, requiring in-clinic monitoring instead.
Product
Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0973-2022·2022-04-27
Artis zeego X-ray imaging system recalled for insufficient cooling
Siemens is recalling 183 Artis zeego X-ray imaging systems due to a cooling system defect that may prevent adequate X-ray tube cooling, triggering automatic system shutdown.
Product
Artis zeego, Model Number 10280959
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1007-2022·2022-04-27
New England Beach Pizza Recalled for Potential Metal Contamination
Beach Brand Foods is recalling New England Beach Pizza products due to potential metal contamination. The affected lots include Lot 087 with best-by date 11/09/2022, distributed in New Hampshire and Massachusetts.
Product
New England Beach Pizza 1. Extra Cheese 2. Cheese
Category
Food
Distribution
2 states
HighFDA (Drugs)·D-0774-2022·2022-04-27
Injectable Rifampin Recalled Due to Failed Quality Specifications
Mylan Pharmaceuticals is recalling injectable Rifampin vials nationwide due to failed impurities and degradation specifications discovered during stability testing.
Product
RIFAMPIN — RIFAMPIN (RIFAMPIN)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V282000·2022-04-27
Commercial buses with inoperative collision system lack required warning label
Navistar is recalling certain 2022-2023 commercial buses equipped without forward radar units. The required warning label indicating the collision mitigation system is inoperative may be missing, increasing crash risk.
Product
INTERNATIONAL — INTERNATIONAL, IC BUS HV, MV, RE
Category
Vehicle
Distribution
Distributed nationwide

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25826–25850 of 90145