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

40376–40400 of 40480

HighFDA (Devices)·Z-1866-2012·2012-07-04
Stryker Endoscopy Recalls Formula Shaver Handpieces Due to Routine Check Concerns
Stryker Endoscopy is recalling 34 Formula and Formula 180 Shaver Handpieces because routine checks to ensure accuracy and fitness for use may not have been adequately determined.
Product
Formula Shaver Handpiece (with buttons); Formula 180 Shaver Handpiece (with button) Rx only, Made USA.: Stryker Endoscopy 5900 Optical Court San Jose, CA 95138 Components within the Crossfire System that provided abrasion, resection, debridement and removal of bone and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1877-2012·2012-07-04
Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance
Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that could be dislodged.
Product
SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 14-GAUGE WHITE NEEDLE,RECTANGULAR FLANGE AND SUTURE COLLAR, 6" (15CM) LONG Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1885-2012·2012-07-04
Terumo Recalls Sarns Cardioplegia Cannulas Due to Foreign Substance
Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that can be dislodged.
Product
MAYO MN XCOATED 3/8X1/2 AV Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1873-2012·2012-07-04
Colgate 360 Toothbrush Recalled Due to Battery Cap Defect
Colgate-Palmolive is recalling 280,044 units of Colgate 360 battery-powered toothbrushes because the battery cap may blow off the handle.
Product
Colgate 360 Replaceable Head Battery Powered Toothbrush Soft UPC 03500068747 Dist. by Colgate-Palmolive Co. New York, NY 10022 Made in China. For teeth cleansing.
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1881-2012·2012-07-04
Terumo Recalls Sarns Antegrade Cardioplegia Cannula Due to Foreign Substance
Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulae because a foreign substance was found on the inner surface of some tips that could be dislodged.
Product
XC HEART/LUNG PACK W/SX25RX Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1859-2012·2012-07-04
Stryker Recalls GoBed+ Model FL20E Hospital Beds Due to Scale Failures
Stryker is recalling 6,325 GoBed+ Model FL20E hospital beds worldwide because loadcell failures can cause scale errors or disable bed exit functions.
Product
GoBed+ . Model FL20E Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1887-2012·2012-07-04
Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance
Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that can be dislodged.
Product
X-COATED H/L PK W/FX15RW40 Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1872-2012·2012-07-04
Colgate 360 Toothbrush Recalled Due to Battery Cap Defect
Colgate-Palmolive is recalling 280,044 Colgate 360 battery-powered toothbrushes because the battery cap may blow off the handle.
Product
Colgate 360 Replaceable Head Battery Powered Toothbrush Medium UPC03500068750 Dist. by Colgate-Palmolive Co. New York, NY 10022 Made in China. For teeth cleansing.
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1864-2012·2012-07-04
Hill-Rom Recalls Advanta 2 Hospital Beds Due to Siderail Screw Stripping
Hill-Rom is recalling 7,843 Advanta 2 hospital beds because screws used to attach siderails were found to be stripping from the plastic cavity.
Product
Advanta 2 Bed. The Advanta 2 Bed is intended for low to moderate acuity patients in the medical/surgical area of the hospital.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1878-2012·2012-07-04
Terumo Recalls Sarns Antegrade Cardioplegia Cannulas Due to Foreign Substance
Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that could be dislodged.
Product
SARNS ANTEGRADE CARDIOPLEGIA CANNULA: ROOT INFUSION CANNULA WITH 12-GAUGE BLUE NEEDLE,RECTANGULAR FLANGE AND SUTURE COLLAR, 6" (15CM) LONG Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1890-2012·2012-07-04
Terumo Recalls Sarns Antegrade Cardioplegia Cannula Kits Due to Foreign Substance
Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannula kits because a foreign substance was found on the inner surface of some cannula tips that could be dislodged.
Product
CPB CATHETER KIT- DR OWEN Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1874-2012·2012-07-04
Colgate 360 Toothbrush Heads Recalled Due to Battery Cap Defect
Colgate-Palmolive is recalling 280,044 units of Colgate 360 Replaceable Head Battery Powered Bonus Twin Pack Toothbrushes because the battery cap can blow off.
Product
Colgate 360 Replaceable Head Battery Powered Bonus Twin Pack Toothbrush Soft UPC 03500068762 Dist. by Colgate-Palmolive Co. New York, NY 10022 Made in China. For teeth cleansing.
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1880-2012·2012-07-04
Terumo Recalls Sarns Cardioplegia Cannulas Due to Foreign Substance
Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance on the inner surface of the tips can be dislodged during use.
Product
INDIANA/OHIO HEART Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1867-2012·2012-07-04
Siemens BCS Behring Coagulation System Recalled for Potential Test Errors
Siemens Healthcare Diagnostics is recalling 186 BCS Behring Coagulation Systems because a specific sequence of tests may result in shortened clotting times.
Product
BCS(R) Behring Coagulation System, Device catalog No. OVIO03 Product Usage: Multipurpose system for In Vitro coagulation studies
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1891-2012·2012-07-04
Terumo Recalls Sarns Cardioplegia Cannulas Due to Foreign Substance
Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance was found on the inner surface of some tips that can be dislodged.
Product
CPB CATHETER KIT- DR HENDRICKSO Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1861-2012·2012-07-04
Stryker Rose Bed Recall Due to Loadcell Failure in Scale Function
Stryker is recalling Rose Model FL14E beds because loadcell failures cause scale errors and disabled bed exit functions.
Product
Stryker Rose Bed Model (FL14E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1879-2012·2012-07-04
Terumo Recalls Sarns Cardioplegia Cannulas Due to Foreign Substance
Terumo CVS is recalling Sarns Antegrade Cardioplegia Cannulas because a foreign substance on the inner surface may dislodge during use.
Product
FX PACK Product Usage: The Sarns Cardioplegia Cannula and Cardioplegia/Vent Catheters are indicated for placement in the aortic root to deliver cardioplegia solution or blood to the heart, to vent the left heart, and to aspirate air from the aorta during cardiopulmonary…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1904-2012·2012-07-04
Abbott Recalls Architect CA 19-9 Reagent Kits Due to Result Shifts
Abbott Laboratories is recalling specific lots of ARCHITECT CA 19-9XR Reagent Kits because they are causing an upward shift in patient test results.
Product
ARCHITECT CA 19-9XR Reagent Kit; ARCHITECT CA 19-9 Reagent Kit, list 291-20 (4 x 100 tests), 2K91-25 and 2K91-27 (1 x 100 tests); Product Usage: The ARCHITECT CA 19-9XR assay is a chemiluminescent microparticle immunoassay (CMIA) for the quantitative determination of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1895-2012·2012-07-04
Zimmer Recalls Shoulder Surgery Drill Due to Labeling Error
Zimmer, Inc. is recalling 87 units of a shoulder surgery drill because the catalog number on the packaging did not match the actual product.
Product
Bigliani/Flatow The Complete Shoulder Solution Trabecular Metal Glenoid Instrument Drill with Stop, 6 mm; the products are medical instruments intended for use when performing surgery of the shoulder.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1863-2012·2012-07-04
Stryker Recalls Go Bed II+ Model FL 28 Ex Due to Scale Failures
Stryker is recalling 9,440 Go Bed II+ Model FL 28 Ex hospital beds due to an abnormally high failure rate of loadcells, which can cause scale errors or disabled functions.
Product
Go Bed II+ Model FL 28 Ex Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1871-2012·2012-07-04
Colgate Adult Motion Whitening Battery Toothbrush Recalled for Battery Cap Defect
Colgate-Palmolive is recalling Adult Motion Whitening Battery Toothbrushes because the battery cap can be forcibly blown off the handle.
Product
Colgate Adult Motion Whitening Battery Toothbrush UPC 035000691507 Dist. by Colgate-Palmolive Co. New York, NY 10022 Made in China. For teeth cleansing.
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1862-2012·2012-07-04
Stryker MA204 Bed Recall Due to Loadcell Failure in Scale Function
Stryker is recalling MA204 beds because loadcells in the scale and bed exit systems are failing at an abnormally high rate.
Product
Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1868-2012·2012-07-04
MedComp 8F Plastic Pro-Fuse CT Low Profile Port Recall
Medical Components, Inc. is recalling 30 kits of the MedComp 8F Plastic Pro-Fuse CT Low Profile Port because the kits contain the wrong port model.
Product
MRCTT80041 MedComp 8F Plastic Pro-Fuse(R) CT Low Profile Port with Attachable Chronoflex(R) Polyurethane Catheter. Power Injectable Implantable Infusion Port insertion kit.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1898-2012·2012-07-04
Salter Labs Recalls Adult Divided Cannula Due to Connector Mismatch
Salter Labs is recalling 242 cases of adult divided cannulas because some units labeled with male luer lock connectors actually contained female luer lock connectors.
Product
Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7 ft, oxygen tube, 7 ft. CO2 tube RX only.For Single Patient Use only. Distributed by Tri-Anium Assembled in Mexico. Usage: Delivery of Anesthesia.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1902-2012·2012-07-04
Sekisui Recalls 1,600 Acetaminophen Assay Kits Due to Reagent Discoloration
Sekisui Diagnostics is recalling 1,600 MULTIGENT Acetaminophen assay kits distributed in Illinois because discoloration of the enzyme reagent causes erratic test results.
Product
MULTIGENT Acetaminophen for use with Architect/Aeroset Cat. No. 2K99-20. Assay is intended for the quantitative determination of acetaminophen in human serum or plasma.
Category
Medical Device
Distribution
1 state

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40376–40400 of 40480