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

22376–22400 of 25981

HighFDA (Devices)·Z-0712-2022·2022-03-09
KWIK-STIK Quality Control Kit Recalled for Incorrect Antibiotic Susceptibility
Microbiologics Inc is recalling KWIK-STIK quality control kits containing Enterococcus faecalis because certain lots are susceptible to Gentamicin Synergy when they should be resistant. The defect could affect laboratory testing accuracy.
Product
KWIK-STIK, Quality control kit for culture media, sold as: a. KWIK-STIK 2-pack Enterococcus faecalis derived from ATCC 51299 b. KWIK-STIK 6-pack Enterococcus faecalis derived from ATCC 51299
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0696-2022·2022-03-09
MEDLINE Micro-Kill Bleach Germicidal Wipes Recall: Out-of-Specification Sodium Hypochlorite
MEDLINE recalls Micro-Kill Bleach Germicidal Wipes due to out-of-specification low levels of sodium hypochlorite, the active disinfecting ingredient. Affected batches may have reduced effectiveness.
Product
MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0710-2022·2022-03-09
Abbott Alinity m reaction units risk detachment during transport
Abbott Molecular is recalling 3063 kits of Alinity m Integrated Reaction Units due to potential detachment of reaction vessels from the unit cap during transport. No injuries have been reported.
Product
Alinity m Integrated Reaction Units (IRU)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0686-2022·2022-03-09
Titanium Toe Implants Recalled for Incorrect MRI Safety Labeling
BioPro Titanium MPJ toe implants are recalled because labeling incorrectly claims MRI safety without actual testing. Patients should consult their physician before undergoing MRI procedures.
Product
Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM, Part ID 17035
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0721-2022·2022-03-09
Surgical knee navigation implant recalled over sterilization failures
Orthosoft's NavitrackER knee navigation system may lack proper sterilization. The product was distributed without passing required sterilization tests, risking infection.
Product
NavitrackER Kit A: Knee, Model Number 20-8000-000-07,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0655-2022·2022-03-09
Digital Angiography System generator may exceed safe radiation dose rates
Shimadzu recalled 28 Digital Angiography Systems with Generator Model D150GC-40 due to inadequate installation adjustment criteria that may cause x-ray radiation dose rates to exceed safe fluoroscopic imaging limits.
Product
Digital Angiography System Shimadzu Trinias Generator Model: D150GC-40
Category
Medical Device
Distribution
15 states
HighFDA (Devices)·Z-0692-2022·2022-03-09
AU/DxC AU Magnesium Test Kits Recalled Due to Measurement Error in Lipemic Samples
Beckman Coulter is recalling 181,776 AU/DxC AU Magnesium test kits because the test may give falsely elevated results in lipemic samples, potentially affecting clinical interpretation.
Product
AU/DxC AU Magnesium, Catalog/REF Number OSR6189, UDI 15099590010850
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0685-2022·2022-03-09
BioPro Titanium Toe Implant Recalled for Incorrect MRI Safety Claims
BioPro Titanium MPJ toe implants contain incorrect documentation falsely claiming they are MR Conditional without proper testing. Patients should not assume these implants are safe for MRI.
Product
Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG, Part ID 16816
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0714-2022·2022-03-09
Quality Control Kit Bacterial Strain Shows Unexpected Gentamicin Susceptibility
Microbiologics has recalled KWIK-STIK quality control kits due to a specific lot failing to meet resistance specifications for Gentamicin Synergy. The affected bacterial strain showed unexpected susceptibility when it should have been resistant.
Product
KWIK-STIK, Quality control kit for culture media, sold as: KWIK-STIK (single-pack) Enterococcus faecalis derived from ATCC 51299
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0709-2022·2022-03-09
Lacrimedics Collagen Plugs recalled for potential sterility seal compromise
Lacrimedics is recalling Collagen Plugs (models CP3, CP4, CP5) due to potential seal integrity defects in sterile pouches. The seals may contain channels that could compromise sterility and allow contamination.
Product
Collagen Plugs, CP3, 0.3mm, CP4, 0.4mm, CP5, 0.5 mm, Sterile, EO, Rx Only, CE Dry eye treatment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0803-2022·2022-03-09
Ice Cream Mislabeled: Black Walnut Packed in Cookie Dough Container
Signature Select Black Walnut Ice Cream was incorrectly packaged in containers labeled as Cookie Dough, which do not declare nuts as an allergen. The product lid correctly identifies the actual flavor.
Product
Signature Select Cookie Dough Ice Cream Vanilla Flavored ice cream with chocolate flavored chips and chunks of chocolaty chip cookie dough. Artificial Flavor added. 1.5 qt. paper container. 6 retail units per case. UPC 2113008803 Some container were filled with Black Wal
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-0698-2022·2022-03-09
QC Control Panels Fail Shelf Life Stability Test at 24 Months
Microbiologics QC control panels for bacterial diagnostic testing failed shelf life validation at 24 months. The 29 affected units were distributed across US states and internationally to Canada, UK, Australia, Belgium, and India.
Product
Microbiologics QC Sets and Panels. BD MAX" CT/GC/TV Verification and Control Panel. Containing High, Medium and Low Level Controls.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0682-2022·2022-03-09
Titanium Toe Implant Recalled for Incorrect MR Compatibility Claims
BioPro Titanium MPJ toe implants are being recalled due to incorrect statements in device labeling claiming MR Conditional status when MR testing was not performed on the titanium version.
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM, Part ID 16813
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22093·2022-03-09
Danby Free-Standing and Slide-In Ranges Recalled for Tip-Over Hazard
Danby is recalling about 1,700 free-standing and slide-in electric and gas ranges because the anti-tip-over bracket may not be securely installed, creating a tip-over hazard and risk of burn injuries when heavy objects are placed on an open oven door.
Product
Danby brand free-standing and slide-in electric and gas ranges
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0701-2022·2022-03-09
Helix Elite Molecular Standards recalled due to shelf life test failure
Microbiologics Inc is recalling Helix Elite Molecular Standards for Inactivated Influenza A/B and Respiratory Syncytial Virus because shelf life testing failed at 24 months, potentially affecting product stability.
Product
Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Influenza A/B and Respiratory Syncytial Virus
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0702-2022·2022-03-09
da Vinci Surgical Cannula Reducer Metal Tip May Dislodge During Surgery
Intuitive Surgical is recalling the da Vinci Xi and X 12-8 mm Conductive Cannula Reducer because the metal tip may dislodge from the plastic shaft. If unnoticed, additional surgery may be needed, or energy leakage could cause tissue damage.
Product
da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0720-2022·2022-03-09
BUTLER Clear Dip Recalled for Lack of FDA Premarket Clearance
Sunstar Americas is recalling BUTLER Clear Dip nationwide due to lack of FDA premarket clearance. The product was distributed in 22,514 units across multiple lot codes.
Product
BUTLER Clear Dip, 12 bottles/case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0699-2022·2022-03-09
Helix Elite Molecular Reference Standard Recall for Failed Shelf-Life Testing
Microbiologics Inc is recalling Helix Elite Molecular Standards for inactivated RSV A because real-time shelf life testing failed at 24 months, indicating the product may not maintain stability through its claimed expiration date.
Product
Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Respiratory Syncytial Virus A Strain Long. Target pathogens are lyophilized in a PCR compatible matrix, and stable at 2¿C-25¿C through the expiration date. Each lyophilized pellet is packaged in a single-use
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0688-2022·2022-03-09
Titanium Toe Joint Implant Contains False MR Compatibility Claims
BioPro recalled titanium toe implants due to incorrect claims in documentation about magnetic resonance (MR) compatibility testing that was never conducted. The FDA issued a Class II recall to address the misleading safety information.
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0700-2022·2022-03-09
Helix Elite Molecular Standard Fails FDA Shelf-Life Stability Testing
Microbiologics Inc. recalls Helix Elite Inactivated Neisseria gonorrhoeae Strain GL0071 molecular standard after real-time shelf life testing failed at 24 months. The product was distributed nationwide and internationally.
Product
Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Neisseria gonorrhoeae Strain GL0071.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0690-2022·2022-03-09
Titanium Toe Implant Recalled for Incorrect MRI Safety Statements
BioPro is recalling Titanium MPJ toe implants due to false claims of MRI compatibility. The device instruction manual states it is MRI-safe despite not being tested.
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS, Part ID 17197
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0681-2022·2022-03-09
Acorn stairlifts recalled due to inadequate seat structural strength
Acorn Stairlifts Inc. is recalling multiple stairlift models because the seats may not have adequate strength to consistently support users during continued use, creating a fall hazard.
Product
Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0808-2022·2022-03-09
Wegmans Roasted Garlic Hummus Recalled for Potential Plastic Contamination
Wegmans brand Roasted Garlic hummus may contain blue plastic pieces. Affected units were distributed to MD, MA, NJ, NY, NC, PA, and VA.
Product
Wegmans brand Roasted Garlic hummus; NET WT 32 OZ (2 LB) 908 g; packaged in clear plastic container with a clear plastic snap lid; Keep Refrigerated
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-0687-2022·2022-03-09
Titanium Toe Implant Recalled for Incorrect MRI Safety Claims
BioPro Titanium MPJ toe implant documentation incorrectly claims MRI safety testing that was never conducted. The implant is not proven safe for MRI use.
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD, Part ID 17036
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V135000·2022-03-08
2022 Forest River Cardinal travel trailers recalled for electrical fire risk
Forest River is recalling certain 2022 Cardinal and related travel trailers due to a loose wire cord at the 50AMP shore power inlet that may cause an electrical short and fire.
Product
FOREST RIVER — 2022 FOREST RIVER CARDINAL
Category
Vehicle
Distribution
Distributed nationwide

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