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

9526–9550 of 27393

SevereFDA (Devices)·Z-1490-2022·2022-08-17
Crome Implantable Cardioverter Defibrillators may deliver reduced shock energy
Medtronic recalls 866 Crome implantable defibrillators due to potential reduced shock energy delivery during high-voltage therapy, affecting devices worldwide. Patients should contact their physician to determine if their device is affected.
Product
Crome Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D): a. Crome HF CRT-D, Model Numbers: DTPC2D4, DTPC2D1; b. Crome HF Quad CRT-D, Model Numbers: DTPC2QQ, DTPC2Q1
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1400-2022·2022-08-17
Viral Transport Container Distributed Without FDA Clearance or Guidance Compliance
Haimen Shengbang Laboratory Equipment recalled 100,000 viral transport containers distributed without FDA clearance and outside FDA guidance, affecting facilities in California, Florida, Illinois, New York, and China.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Custom Made
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1399-2022·2022-08-17
FDA Recalls 3.95 Million Viral Transport Containers Distributed Without Clearance
The FDA recalled 3.95 million viral transport containers distributed without FDA clearance and in violation of established guidance. The containers were distributed worldwide, including to facilities in California, Florida, Illinois, and New York.
Product
HXBL/WETEX/Genesis Biomedical Viral Transport Container, Model No. HX-K59-1
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1489-2022·2022-08-17
Crome Implantable Cardioverter Defibrillators Recalled for Reduced Shock Energy
Medtronic is recalling 1,657 Crome implantable cardioverter defibrillators due to potential reduced shock energy during high-voltage therapy. Affected devices may deliver only 79% of programmed energy.
Product
Crome Implantable Cardioverter Defibrillators: a. Crome VR ICD, Model Numbers: DVPC3D1, DVPC3D4; b. Crome DR ICD, Model Numbers: DDPC3D1, DDPC3D4
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1488-2022·2022-08-17
Cobalt Implantable Defibrillators May Deliver Reduced Shock Energy
Medtronic Cobalt implantable cardioverter defibrillators may deliver approximately 79% of programmed shock energy during high-voltage therapy. The reduced energy could affect device performance in patients requiring defibrillation.
Product
Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D): a. Cobalt HF CRT-D, Model Numbers: DTPB2D4, DTPB2D1; b. Cobalt HF Quad CRT-D, Model Numbers: DTPB2QQ, DTPB2Q1
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1486-2022·2022-08-17
Medtronic Cobalt Implantable Defibrillators Recalled Due to Reduced Shock Energy Defect
Medtronic has recalled 8,429 Cobalt implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) worldwide due to potential reduced shock energy during therapy, potentially delivering 79% of programmed energy.
Product
Cobalt Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D): a. Cobalt XT HF CRT-D, Model Numbers: DTPA2D4, DTPA2D1; b. Cobalt XT HF Quad CRT-D, Model Numbers: DTPA2QQ, DTPA2Q1
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1485-2022·2022-08-17
Cobalt Implantable Cardioverter Defibrillators recalled for reduced shock energy
Medtronic's Cobalt implantable cardioverter defibrillators may deliver approximately 79% of programmed shock energy during high-voltage therapy. Patients with affected models should contact their physician.
Product
Cobalt Implantable Cardioverter Defibrillators: a. Cobalt XT VR ICD, Model Numbers: DVPA2D1, DVPA2D4; b. Cobalt XT DR ICD, Model Numbers: DDPA2D1, DDPA2D4
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1514-2022·2022-08-17
Lithotripsy Generator Recall Due to Mis-Wired Component Affecting System Reliability
Olympus Corporation recalls 2 units of the ShockPulse-SE Lithotripsy Generator due to a mis-wired component that causes improper power supply noise and EMC non-compliance, potentially affecting device reliability and treatment delivery.
Product
ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1509-2022·2022-08-17
MetaFix hip stem mislabeled with wrong size and batch information
A Corin MetaFix hip stem (size 7 collarless) was incorrectly labeled as a size 3 collared stem with wrong batch information. The labeling error creates risk during surgical implantation.
Product
Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1511-2022·2022-08-17
GE Healthcare CT, PET, and NM Patient Tables May Drop During Service
GE Healthcare patient tables used in CT, PET, and NM systems can drop during service if technicians remove incorrect screws without appropriate supports, potentially injuring service personnel.
Product
Service manuals for the CT, PET, or NM table as follows: GT1700/GT1700V/VT1700, GT2000/VT2000, GT2000x/VT2000x, High Capacity Table, Lite Table, Kunlun Table, Global PET-CT Table, NP Table, P2005AA Table, LCT Table, CTE TWIN TABLE Assy. All devices are patient tables for PET/
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2022·2022-08-17
Xhibit Telemetry Receiver Model 96280 alarm escalation software defect
Xhibit Telemetry Receiver Model 96280 units fail to escalate critical alarms after approximately 25 days of continuous use, including signal loss, low battery, and SpO2 sensor issues. Caregivers may not be aware of device failures.
Product
Xhibit Telemetry Receiver, Model: 96280
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1507-2022·2022-08-17
Haiou Needle Retractable Safety Syringe recalls due to needle detachment risk
Approximately 7,218,000 Haiou Needle Retractable Safety Syringes are being recalled due to needle detachment and retracting mechanism failures that increase needlestick injury risk. The affected product was distributed in California.
Product
Haiou Needle Retractable Safety Syringe with Needle-1ML 23G x 1 (0.6x25mm). 200pcs/Box Intended Use: Disposable sterile needle retractable safety syringe. Catalog Number: NRSS1-23G25
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1510-2022·2022-08-17
FDA Recalls 3D Systems VSP Scapula Marking Guide Due to Design Defect
Medical Modeling, Inc. is recalling the 3D Systems VSP Reconstruction Scapula Marking Guide (Model VSPR-301) because it was incorrectly designed. The device was distributed internationally, including to Germany.
Product
3D Systems VSP Reconstruction, Model: VSPR-301 Product: Scapula Marking Guide (Anatomically Shaped), Rx Only, Non-Sterile
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1506-2022·2022-08-17
HAIOU Retractable Safety Syringes Recalled for Needle Detachment Risk
HAIOU retractable safety syringes are recalled due to reports of needle detachment from the syringe after injection and failure to retract, increasing needle stick injury risk. Approximately 4.05 million units are affected.
Product
HAIOU Needle retractable safety syringe with needle-(1ml syringe with 25G x 1-inch needle} 200 pieces/box. Intended Use: Disposable sterile needle retractable safety syringe. Catalog Number: NRSS1-25G25
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2022·2022-08-17
Roche cobas e801 Analyzer Recall: Software Defect Affects Test Results
Roche is recalling approximately 965 cobas e801 Immunoassay Analyzers nationwide due to a software issue that impacts Pre-Wash test signals and results for six diagnostic assays. No injuries or illnesses have been reported.
Product
cobas e801 Immunoassay Analyzer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1516-2022·2022-08-17
Aeos Robotic Digital Microscope software errors affect autofocus and rebalancing
Aesculap is recalling Aeos Robotic Digital Microscopes (versions 2.7 or earlier) due to application errors affecting rebalancing, recovery, and autofocus. Five units were distributed in Arkansas, Indiana, Nebraska, and North Carolina.
Product
Aeos¿ Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010
Category
Medical Device
Distribution
4 states
SevereFDA (Devices)·Z-1401-2022·2022-08-10
SARS-CoV-2 Rapid Antigen Test Kits Distributed Without FDA Approval
North American Diagnostics is recalling SARS-CoV-2 rapid antigen test kits that were distributed without FDA approval or clearance. Approximately 122,366 units were sold to consumers across multiple US states and internationally.
Product
SARS CoV 2 rapid antigen test kits packaged under the following brands: Oral Rapid Test, Oral Rapid Antigen Test, SML LDT Kits, SML Brand Finished Kits, SML Brand BT Test Kits, SML Brand BT Antigen Test Kit LDT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1494-2022·2022-08-10
Unapproved CustMbite Medical Device Recalled Nationwide Due to Missing FDA Clearance
Dental Choice is recalling 708 units of the CustMbite Model CBT-SRS-UL device nationwide because it was marketed and sold without FDA clearance.
Product
CustMbite, Model Number CBT-SRS-UL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1500-2022·2022-08-10
Craftmatic Legacy Bed Base Recalled for Potential Separation Risk
Craftmatic Industries recalls the Legacy Base for Dual Bed Configurations due to a potential for beds to separate or slip away from one another. The defect poses a risk of unintended bed movement.
Product
Legacy Base for Dual Bed Configurations
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1497-2022·2022-08-10
Merlin 2 PCS programming software for implantable devices recalled
St. Jude Medical recalls Merlin 2 PCS model MER3700, software used to program and interrogate Abbott implantable medical devices.
Product
Merlin.net model MN5000 Software
Category
Medical Device
Distribution
54 states
HighFDA (Devices)·Z-1499-2022·2022-08-10
Craftmatic Model 1 Adjustable Bed Base Recalled for Separation Risk
Craftmatic Industries is recalling the Model 1 Base for Dual Bed Configurations due to a potential for the bed bases to separate or slip apart. This defect could cause dual-configured beds to shift unexpectedly.
Product
Craftmatic Model 1 Base for Dual Bed Configurations
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1502-2022·2022-08-10
UroLift System recalled for potential implant deployment failure
Neotract Inc is recalling 18,722 UroLift Systems due to potential improper implant deployment during use. Patients should contact their healthcare provider.
Product
UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-1482-2022·2022-08-10
PRESTIGE RETRACTION GRASPER recalled due to potential weld separation
The FDA is recalling 399 units of the PRESTIGE RETRACTION GRASPER surgical instrument due to risk of weld separation between the handle and shaft. This defect could cause device malfunction during surgical procedures.
Product
PRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8361-10
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1442-2022·2022-08-10
NanoSight NS300 Medical Device Recalled for Laser Safety Noncompliance
Malvern Panalytical is recalling 507 NanoSight NS300 units due to noncompliance with Class 1 laser safety requirements. The device may not meet established safety standards for laser-based instruments.
Product
NanoSight NS300
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1498-2022·2022-08-10
Atellica CH Iron_2 Diagnostic Device Produces False Microalbumin Results from Reagent Carryover
Siemens Atellica CH Iron_2 in vitro diagnostic devices are being recalled because they produce falsely elevated microalbumin test results when a microalbumin test immediately follows an iron test. No illnesses have been reported.
Product
Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use in the quantitative determination of iron in human serum and (lithium heparin) plasma samples.
Category
Medical Device
Distribution
Distributed nationwide

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9526–9550 of 27393