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

23276–23300 of 26062

HighFDA (Devices)·Z-0443-2022·2022-01-05
Medical Device Aberrometer Systems Affected by Remote Code Execution Vulnerability
AMO Manufacturing's iDesign aberrometer systems (711 units, Models G300 and G301) are vulnerable to remote code execution through the Windows Print Spooler service. An attacker could run arbitrary code with SYSTEM privileges to install programs, access or delete data, or create accounts.
Product
iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States); iDesign Refractive Studio Aberrometer (International) and (United States), Model: G301
Category
Medical Device
Distribution
47 states
HighFDA (Devices)·Z-0419-2022·2022-01-05
da Vinci SP Surgical System Software Energy Delivery Defect
Intuitive Surgical recalls 46 da Vinci SP Surgical systems due to software defect causing potential failure or inadvertent delivery of surgical energy. Issue may require surgeon intervention during procedures.
Product
da Vinci SP Surgical systems with the following Model Name/ Model Number / UDI: ASSY,PSS,SP1098,P4/ 380601-44/ 00886874114605 ASSY,SSC,SP1098,P4/ 380940-44 / 00886874114735 ASSY,VSS,SP1098,P4/ 380941-44 / 00886874114742 SOFTWARE, SYSTEM EMBEDDED RLS, SP1098, B70_P4_B327 (OS4 v4.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0354-2022·2022-01-05
BUBS Naturals Collagen Supplement Recalled for Undeclared Milk
BUBS Naturals Fountain of Youth Formula collagen supplement is recalled nationwide because it contains undeclared milk from an MCT oil powder ingredient. Consumers with milk allergies or sensitivities should not consume this product.
Product
BUBS Naturals Fountain of Youth Formula; Collagen Protein; Support for Hair, Skin & Nails; Biotin, Antioxidant, Vitamin C; Maqui Berry Net Wt. 10.16 oz. (288 g)
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0426-2022·2022-01-05
VIDAS Clostridium Difficile GDH test substrate error causes test failure
bioMerieux recalls VIDAS Clostridium Difficile GDH diagnostic test kits due to a substrate error that prevents test execution. Affected users must retest samples, potentially delaying results.
Product
VIDAS Clostridium Difficile GDH, REF 30125-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0418-2022·2022-01-05
Percept PC Implantable Neurostimulator May Become Unresponsive During Cardioversion
The Model B35200 Percept PC Neurostimulator may become unresponsive during cardioversion procedures when circuit electronics are damaged. Affected patients should contact their healthcare provider.
Product
Model B35200 - Percept PC BrainSense Implantable Neurostimulator
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22043·2022-01-05
CRT Motor Youth All-Terrain Vehicles Recalled for Crash Hazard
CRT Motor is recalling about 100 youth ATVs sold at Motorsports Planet because they do not meet mandatory safety requirements and can exceed maximum speed, increasing crash risk.
Product
CRT Motor Youth All-Terrain Vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0441-2022·2022-01-05
Cancer treatment linear accelerator systems recalled for wrong-site dosing risk
Siemens recalled 13 ARTISTE linear accelerator systems for cancer treatment due to a potential safety issue that could cause radiation to be delivered to the wrong treatment site.
Product
ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray photon and electron radiation for the therapeutic treatment of cancer. Model Number: 8162815
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0353-2022·2022-01-05
Raw Tuna at Meat Counter Recalled for High Histamine Levels
Sant' Elia Operations is recalling raw tuna sold at meat counters in Wisconsin because samples tested above 50 ppm histamine, which can cause illness if consumed.
Product
Tuna, raw sold at meat counter and wrapped in butcher paper at point of purchase.
Category
Food
Distribution
1 state
HighFDA (Food)·F-0355-2022·2022-01-05
Giant Eagle Diced Green Peppers Recalled for Listeria Contamination
Giant Eagle, Inc. is recalling frozen diced green peppers (10 oz., Best By 10/14/2023) distributed to stores in Maryland, Pennsylvania, West Virginia, Ohio, and Indiana because the product tested positive for Listeria monocytogenes.
Product
Giant Eagle Diced Green Peppers, 10 oz. 283 g, Frozen bag, 12 packages per case , Best By 10/14/2023 .
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-0429-2022·2022-01-05
VIDAS Mumps IgG diagnostic test kit recalled due to substrate error
bioMerieux is recalling one lot of VIDAS Mumps IgG diagnostic tests because a substrate error prevents the tests from running, causing delays.
Product
VIDAS Mumps IgG (MPG), REF 30218
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0428-2022·2022-01-05
VIDAS procalcitonin diagnostic test substrate error causes testing delays
Nationwide recall of VIDAS procalcitonin test kits for substrate defects that prevent testing and require retesting, potentially delaying diagnostic results.
Product
VIDAS B.R.A.H.M.S. PROCALCITONIN PCT, REF 30450-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0420-2022·2022-01-05
Ultimum Hemostasis Introducer devices recalled due to manufacturing error
Abbott is recalling one lot of Ultimum Hemostasis Introducer devices due to a manufacturing error that resulted in incorrect hub and length. Affected devices are 12 cm long instead of the intended 5 cm.
Product
Ultimum HEMOSTASIS INTRODUCER 5f 1.67 MM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0439-2022·2022-01-05
VIDAS SARS-COV-2 Diagnostic Test Recalled for Substrate Error
bioMerieux is recalling two lots of VIDAS SARS-COV-2 IgG diagnostic tests due to substrate errors that prevent test execution, requiring users to repeat testing and potentially delaying results.
Product
VIDAS SARS-COV-2 IgG, Ref 423834-01
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22044·2022-01-05
Native Creation Small Wool Sweaters Recalled for Lead Paint on Zipper
Native Creation is recalling approximately 170 small wool sweaters for children sizes 0 to 8 because the zipper pull contains lead paint that exceeds federal limits and poses a toxic ingestion risk to young children.
Product
Native Creation Small Wool Sweaters
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0423-2022·2022-01-05
Speech Generation Device Charging Components Recalled for Fire and Electric Shock Hazard
Forbes Rehab Services is recalling Monoprice charging cables and iClever charging bricks for ProSlate Speech Generation Devices due to fire and electric shock risks if cables are damaged or charging occurs near moisture.
Product
Affected components are limited to the Monoprice charging cable (Product # 4867) and 24W iClever Boost Cube charging brick components for the SoundPOD Bluetooth Speaker accessory to the ProSlate Speech Generation Devices (including Proslate 13: B398PS130; Proslate 10: B398PS100;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0430-2022·2022-01-05
VIDAS Measles IgG Test Kit Recalled Due to Substrate Error
bioMerieux is recalling VIDAS Measles IgG test kits due to a substrate error that prevents the test from running, requiring users to repeat testing and potentially delaying results.
Product
VIDAS Measles IgG (MSG), REF 30219
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0435-2022·2022-01-05
VIDAS Estradiol II Test Device Recalled Due to Substrate Error
bioMerieux is recalling one lot of VIDAS Estradiol II diagnostic test devices due to a substrate error that prevents tests from running, causing delayed results and requiring repeat testing.
Product
VIDAS Estradiol II, REF 30431-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0444-2022·2022-01-05
Catalys Precision Laser System recalled for remote code execution vulnerability
AMO Manufacturing is recalling Catalys Precision Laser Systems due to a Windows Print Spooler vulnerability that could allow unauthorized remote code execution with system privileges.
Product
Catalys Precision Laser System, Models: Catalys-U (United States), Catalys-I (International), Catalys-C (China); and Catalys Precision Laser System No Bed, Models: 0160-6020 (United States), 0160-6010 (International)
Category
Medical Device
Distribution
47 states
HighFDA (Drugs)·D-0322-2022·2022-01-05
Norepinephrine Injection Recalled Due to Lack of Sterility Assurance
SterRx is recalling 36,576 bags of Norepinephrine 16 mg per 250 mL injection (0.9% Sodium Chloride) distributed nationwide because the manufacturer cannot assure the product meets sterility requirements.
Product
NOREPINEPHRINE, 16 mg per 250 mL, (64 mcg per mL) in 0.9% Sodium Chloride Injection, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-926-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0440-2022·2022-01-05
Siemens Atellica CH β2-Microglobulin Assay Lot 211446 Recalled for Measurement Bias
Siemens Healthcare Diagnostics recalled lot 211446 of the Atellica CH β2-Microglobulin assay due to analytical bias in test results. The assay showed positive bias up to 20.9% at some concentrations and negative bias up to 10.5% at others.
Product
Atellica CH ¿2-Microglobulin (B2M) -M) Assay for in vitro diagnostic use in the quantitative determination of ¿2-microglobulin in human serum and plasma Siemens Material Number (SMN): 11097635
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0288-2022·2021-12-29
Moxifloxacin 1 mg/mL Solution Label Mix-up Recall
Denver Solutions, LLC (doing business as Leiters Health) is recalling Moxifloxacin 1 mg/mL intracameral injection solution because vials labeled as 1 mg/mL may actually contain 5 mg/mL, creating a serious dosing error risk.
Product
Moxifloxacin, 1 mg/mL, 1mL in 2mL vial, solution for intracameral injection, 10 vials/carton, Rx only, Leiters 13796 Compark Blvd, Englewood, CO 80112, (800) 292-6772, NDC 71449-096-42
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0350-2022·2021-12-29
Dakota Tom's Chicken Salad Croissant Sandwiches Recalled for Undeclared Allergens
Dakota Tom's and Market Fresh branded Chicken Salad Croissant sandwiches are being recalled because they contain undeclared egg and milk. Consumers who have allergies to these ingredients should not consume the product.
Product
Dakota Tom's and Market Fresh branded Chicken Salad Croissant sandwiches. Net Wt. 6.5 oz. UPC 37296-10100, Dakota Toms, Box 271, Corsica, SD 57328.
Category
Food
Distribution
4 states
SevereFDA (Drugs)·D-0292-2022·2021-12-29
OTC Expectorant Recall: Microbial Contamination in Rompe Pecho
Efficient Laboratories is recalling Rompe Pecho guaifenesin expectorant in 4 fl oz and 6 fl oz bottles due to microbial contamination of non-sterile products. The affected product was distributed nationwide.
Product
ROMPE PECHO — ROMPE PECHO (GUAIFENESIN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0293-2022·2021-12-29
OTC Cough and Cold Drug Recalled for Microbial Contamination
Efficient Laboratories is recalling approximately 4,026 bottles of Rompe Pecho Max Multi-Symptoms cough and cold medicine nationwide due to potential microbial contamination of the non-sterile product.
Product
ROMPE PECHO MAX MULTI SYMPTOMS — ROMPE PECHO MAX MULTI SYMPTOMS (ACETAMINOPHEN, DEXTROMETHOPHAN HBR, PHENYLEPHRINE HCL, GUAIFENESIN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0394-2022·2021-12-29
WIRION Embolic Protection System Filter Withdrawal Difficulties
Cardiovascular Systems Inc recalls WIRION Embolic Protection System devices (6Fr) because the filter assembly may become difficult to withdraw, and the device may tear or separate, creating a risk of blood clot embolization.
Product
WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6
Category
Medical Device
Distribution
38 states

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23276–23300 of 26062