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

39001–39025 of 40449

ModerateFDA (Devices)·Z-0739-2013·2013-02-06
Becton Dickinson Recalls BBL Fildes Enrichment Tubes for Growth Failure
Becton Dickinson is recalling BBL Fildes Enrichment tubes because they may fail to support the growth of Haemophilus species, potentially affecting laboratory test results.
Product
BBL(TM) Fildes Enrichment, catalog number 211866, 10 tubes/pack, labeled in part ***Becton Dickinson and Company, Sparks, MD 21152 USA*** Intended Use: Fildes Enrichment may be used to enrich a variety of media for the cultivation of various microorganisms. Fildes Enrichment…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0764-2013·2013-02-06
MOOG Infinity Enteralite Feeding Pumps Recall for Manual Addendum
MOOG Medical Devices Group is recalling 92,488 Infinity Enteralite Ambulatory Feeding Pumps to add an operator's manual addendum regarding the Infinite Dose mode and air-in-line detection limitations.
Product
Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: provide a means for the volumetric delivery of fluids used in Enteral applications.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0743-2013·2013-02-06
Alfa Wassermann System Diluent Recalled for Inaccurate Calibration Results
Alfa Wassermann is recalling 4,104 kits of System Diluent because inorganic phosphorus assays may not produce acceptable calibration results.
Product
Alfa Wassermann System Diluent 750 mL Manufactured for Alfa Wassermann Diagnostic Technologies LLC 4 Henderson Drive West Caldwell, NJ 07006 Alfa Wassermann B.V. Pompmolenlaan 24 3447 GK, Woerden The Netherlands Common name is water solution. Intended to dilute…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0751-2013·2013-02-06
Greatbatch Medical Recalls 45 Degree Angle Drivers for Noisy Operation
Greatbatch Medical is voluntarily recalling 913 Small Angled Driver 45 units worldwide due to reports of noisy or rough operation.
Product
45¿ Angle Driver / Z-H, Greatbatch Medical 10 000 Wahrie Drive, Clarance, NY 14031. Model #: P2661, P2662, T3635, T5586,T6031, T6164,T10161, T12628,T14879, T16422,T2487,T2713,T116057, T13635, MPU260045AO01, MPU260045ZH01. The Driver is intended to act as an interface…
Category
Medical Device
Distribution
8 states
ModerateFDA (Devices)·Z-0702-2013·2013-02-06
Philips Juno DRF X-ray System Recalled for Display Compliance Issues
Philips Healthcare is recalling 16 Juno DRF X-ray systems because fluoroscopy dose values may not display correctly at the operator's position.
Product
Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose Model: 70920 Product Usage: Universal R/F, general use
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0755-2013·2013-02-06
Ortho VITROS Vapor Adsorption Cartridges Recalled for Incorrect Packaging
Ortho-Clinical Diagnostics is recalling VITROS Vapor Adsorption Cartridges because some cartons incorrectly contain Particulate Cartridges, which may bias test results.
Product
Ortho Clinical Diagnostics VITROS¿ Chemistry Products Vapor Adsorption Cartridge REF/CAT No. 680 0100. VITROS¿ Vapor Adsorption Cartridges are used to remove vapor contaminants that may potentially interfere with Signal Reagent used with MicroWell Assays on the VITROS¿ 3600…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0745-2013·2013-02-06
Siemens Dimension IRON Calibrator Recalled for Calibration Slope Issues
Siemens Healthcare Diagnostics is recalling Dimension IRON Calibrators because some lots produced calibration results outside acceptable ranges.
Product
Dimension(R) IRON Calibrator (DC85), Siemens material number 10445010. The Dimension(R) IRON Calibrator is an in vitro diagnostic product intended to be used to calibrate the Iron method for the Dimension(R) clinical chemistry system.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0747-2013·2013-02-06
Alere Cholestech LDX Calibration Verification Recall for HDL Errors
Alere San Diego, Inc. is recalling 614 kits of Cholestech LDX Calibration Verification due to out-of-range HDL cholesterol results.
Product
Alere Cholestech LDX Calibration Verification, 4 vial set, Catalog Number: 88770 Alere Cholestech LDX Calibration Verification (hereafter referred to as CAL VERS) enables users to monitor the performance of total cholesterol (TC), high density lipoprotein cholesterol (HDL)…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0746-2013·2013-02-06
Alere Cholestech LDX Multianalyte Control Recalled for HDL Errors
Alere San Diego, Inc. is recalling Alere Cholestech LDX Multianalyte Control kits because they may produce out-of-range HDL cholesterol results.
Product
Alere Cholestech LDX Multianalyte Control, 2 vial set, Catalog Number: 88769 Alere Cholestech LDX Multianalyte Control (hereafter referred to as Controls) enables users to monitor the performance of total cholesterol (TC), high density lipoprotein cholesterol (HDL)…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0712-2013·2013-01-30
DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation
DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.
Product
DePuy Spine VIPER POLY SCREW 5.5 10 X 80MM Tl Product Code: 1867-15-180 Spinal Implant Component.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0705-2013·2013-01-30
DePuy Spine VIPER Polyaxial Screw Recall for Potential Separation
DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.
Product
DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Product Code: 1867-15-870 Spinal Implant Component.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0708-2013·2013-01-30
DePuy Spine VIPER Polyaxial Screw Recall for Potential Disassociation
DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.
Product
DePuy Spine VIPER POLY SCREW 5.5 9 X70MM Tl Product Code: 1867-15-970 Spinal Implant Component.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0713-2013·2013-01-30
DePuy Spine VIPER Polyaxial Screws Recalled for Potential Component Separation
DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.
Product
DePuy Spine VIPER POLY SCREW 5.5 10X100MM Tl Product Code: 1867-15-199 Spinal Implant Component.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0706-2013·2013-01-30
DePuy Spine Recalls VIPER Polyaxial Screws Due to Potential Separation
DePuy Spine is recalling 36 units of VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.
Product
DePuy Spine VIPER POLY SCREW 5.5 8 X80MM Tl Product Code: 1867-15-880 Spinal Implant Component.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0711-2013·2013-01-30
DePuy Spine VIPER Polyaxial Screws Recalled for Potential Disassociation
DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.
Product
DePuy Spine VIPER POLY SCREW 5.5 10 X 70MM Tl Product Code: 1867-15-170 Spinal Implant Component.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0710-2013·2013-01-30
DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation
DePuy Spine is recalling VIPER polyaxial screws because the shank may separate from the head during high-torque insertion.
Product
DePuy Spine VIPER POLY SCREW 5.5 9 X100MM Tl Product Code: 1867-15-999 Spinal Implant Component.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0707-2013·2013-01-30
DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation
DePuy Spine is recalling VIPER Polyaxial Screws because the screw shank may separate from the head during high-torque insertion.
Product
DePuy Spine VIPER POLY SCREW 5.5 8 X100MM Tl Product Code: 1867-15-899 Spinal Implant Component.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0709-2013·2013-01-30
DePuy Spine VIPER Polyaxial Screws Recalled for Potential Separation
DePuy Spine is recalling VIPER Polyaxial Screws 8x80mm and larger because the screw shank may separate from the head during high-torque insertion.
Product
DePuy Spine VIPER POLY SCREW 5.5 9 X 80MM Tl Product Code: 1867-15-980 Spinal Implant Component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0721-2013·2013-01-30
ConMed Recalls Goldvac UltraClean Accessory Electrodes Due to Compromised Sterile Seals
ConMed is recalling Goldvac UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.
Product
Goldvac(TM) UltraClean(R) Accessory Electrode 6 inch Coated Blade with Extended Insulation, REF/Catalog No. 60-7523-001, Sterile, Rx ONLY -- CONMED CORPORATION, Electrosurgical, Cutting and Coagulation and Accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0733-2013·2013-01-30
ConMed Recalls UltraClean Accessory Electrode Due to Compromised Sterile Seals
ConMed is recalling UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.
Product
UltraClean(R) Accessory Electrode 6 inch Coated Blade, REF/Catalog No. 139107, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION, Electrosurgical, Cutting and Coagulation and Accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0736-2013·2013-01-30
ConMed Recalls UltraClean Accessory Electrode Blades Due to Seal Compromise
ConMed is recalling UltraClean Accessory Electrode 4 inch Coated Blades because some sterile pouch seals were compromised. No illnesses or injuries have been reported.
Product
UltraClean(R) Accessory Electrode 4 inch Coated Blade, REF/Catalog No. 139112, Single Use, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0724-2013·2013-01-30
ConMed Recalls ABC Nozzles Due to Compromised Sterile Pouch Seals
ConMed is recalling 313,190 ABC Nozzles because some sterile pouch seals were compromised. No illnesses or injuries have been reported.
Product
ABC(R) NOZZLE, Single Patient Use Nozzle, (For use with 130500 Reusable ABC(R) Handpiece), REF/Catalog No. 130343, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0722-2013·2013-01-30
ConMed Recalls Goldvac UltraClean Accessory Electrode Due to Compromised Sterile Seals
ConMed is recalling Goldvac UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.
Product
Goldvac(TM) UltraClean(R) Accessory Electrode 4 inch Coated Blade, REF/Catalog No. 60-7524-001, Sterile, Rx ONLY -- CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0729-2013·2013-01-30
ConMed Recalls UltraClean Accessory Electrodes Due to Compromised Sterile Seals
ConMed is recalling UltraClean Accessory Electrodes because some sterile pouch seals were compromised. No illnesses or injuries have been reported.
Product
UltraClean(R) Accessory Electrode, 1 inch Coated Blade, REF/Catalog No. 139100, Single Use, Sterile, Rx ONLY --CONMED CORPORATION, Electrosurgical, Cutting and Coagulation and Accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0728-2013·2013-01-30
ConMed Recalls Electrosurgical Tip Cleaners Due to Compromised Sterile Seals
ConMed is recalling 313,190 Electrosurgical Tip Cleaners because some sterile pouch seals were compromised. No illnesses or injuries have been reported.
Product
Electrosurgical Tip Cleaner, REF/Catalog No. 138029, Single Use, Sterile, Rx ONLY -- Distributed By: CONMED CORPORATION Electrosurgical, Cutting and Coagulation and Accessories.
Category
Medical Device
Distribution
Distributed nationwide

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39001–39025 of 40449