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

27051–27075 of 27722

SevereFDA (Devices)·Z-0297-2013·2012-11-28
Biomet 3i Recalls OSSEOTITE Dental Implants Due to Shallow Hex Depth
Biomet 3i is recalling 191 OSSEOTITE dental implants because a manufacturing defect makes the internal hex too shallow, which may prevent the driver or abutment from fully engaging.
Product
Product is Full OSSEOTITE 2 Tapered Certain Implant, Model Number XIFNT413, and size 4 x 13 mm. The product is sterile. Product provides a means for prosthetic attachment in single tooth restorations and in partially or fully edentulous spans with multiple single teeth…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0354-2013·2012-11-28
NuVasive Recalls 5.5mm Cannulated Screw Shanks Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 5.5mm x 55mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
5.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0358-2013·2012-11-28
NuVasive Recalls 6.5mm Cannulated Screw Shanks Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 6.5mm x 45mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
6.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0360-2013·2012-11-28
NuVasive Recalls 6.5mm Cannulated Screw Shank Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 6.5mm x 55mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
6.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0349-2013·2012-11-28
NuVasive Recalls 5.5mm Cannulated Screw Shanks Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 5.5mm x 30mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
5.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0357-2013·2012-11-28
NuVasive Recalls 6.5mm Cannulated Screw Shanks Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 6.5mm x 40mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
6.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0378-2013·2012-11-28
NuVasive Recalls 7.5mm Noncannulated Screw Shanks Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 7.5mm x 50mm Noncannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
7.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0352-2013·2012-11-28
NuVasive Recalls 5.5mm Cannulated Screw Shanks Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 5.5mm x 45mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
5.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0373-2013·2012-11-28
NuVasive Recalls 6.5mm Noncannulated Screw Shanks Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 6.5mm x 40mm Noncannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
6.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0375-2013·2012-11-28
NuVasive Recalls 6.5mm Noncannulated Screw Shank Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 6.5mm x 50mm Noncannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
6.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0368-2013·2012-11-28
NuVasive Recalls 4.5mm Noncannulated Screw Shanks Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 4.5mm x 35mm Noncannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
4.5mm x 35mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0290-2013·2012-11-28
Mindray A3 Anesthesia Delivery System Recalled for Potential System Leak
Mindray is recalling 69 A3 Anesthesia Delivery Systems due to a potential system leak caused by a carbon dioxide absorber canister gasket issue.
Product
Mindray A3 Anesthesia Delivery System Manufactured in China for Mindray DS USA Inc. 800 MacArthur Boulevard, Mahwah, NJ 07430 This is a device used to administer to a patient continuously or intermittently a general inhalation anesthetic and to maintain a patient's…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0355-2013·2012-11-28
NuVasive Recalls 6.5mm Cannulated Screw Shank Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 6.5mm x 30mm Cannulated Screw Shanks because the tulip portion may disengage from the shank after implantation.
Product
6.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0369-2013·2012-11-28
NuVasive Recalls 4.5mm Noncannulated Screw Shanks Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 4.5mm x 40mm Noncannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
4.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0351-2013·2012-11-28
NuVasive Recalls 5.5mm Cannulated Screw Shanks Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 5.5mm x 40mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
5.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0419-2013·2012-11-28
King Systems Recalls Child Silicone Laryngeal Airway Devices Due to Sterilization Indicator Defect
King Systems Corp. is recalling 2,630 child silicone laryngeal airway devices because sterilization indicators failed to change color as expected, raising concerns about proper EtO sterilization.
Product
KING LAD SILI CONE SINGLE USE, King Systems, 10 devices/case, ETO Sterile Size 3 / Child Silicone King LAD¿ Patient Size: 30-50kg Product Usage: Laryngeal airway
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0403-2013·2012-11-28
Spacelabs Qube Compact Patient Monitor Recalled for Input Circuit Failure
Spacelabs Healthcare is recalling Qube Compact Patient Monitors because the input circuit may fail, causing the device to shut down when batteries deplete or fail to turn on.
Product
qube Compact Monitor (Patient Monitor) 91390. The monitor is 26.2 cm x 31.5 cm x 13.2 cm and weighs 4.1 kg (10.3 inches x 12.4 inches x 5.2 inches - 9 lbs). It has a 26.2 cm (12.1 inches) LCD display with 1024 x 768 resolution. The Spacelabs Healthcare Qube Compact…
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0428-2013·2012-11-28
IMRIS OR Tables Recalled Due to Magnet Attraction Risk
IMRIS is recalling ORT100 and ORT200 tables used in MRI systems because the foot end may be attracted to the magnet, posing a risk of injury to patients and operators.
Product
IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00), are tables used in both the Neuro II-SE and Neuro III-SV Magnetic Resonance Imaging Systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0407-2013·2012-11-28
Vital Signs Temperature Probe Recalled for Potential Nosebleed Risk
Vital Signs Colorado Inc. is recalling 243,685 disposable temperature probes due to a potential risk of nosebleeds during use.
Product
Vital Signs Disposable General Purpose 9 French Temperature Probe For monitoring of core temperature
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0298-2013·2012-11-28
Biomet 3i Recalls OSSEOTITE Dental Implants Due to Shallow Hex Depth
Biomet 3i is recalling 76 OSSEOTITE dental implants because a manufacturing defect makes the internal hex too shallow, potentially preventing proper engagement of drivers or abutments.
Product
Product is Full OSSEOTITE Parallel Walled Certain Implant, Model Number IFOA411. The product is sterile. Product provides a means for prosthetic attachment in single tooth restorations and in partially or fully edentulous spans with multiple single teeth utilizing delayed or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0370-2013·2012-11-28
NuVasive Recalls 5.5mm Noncannulated Screw Shanks Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 5.5mm x 40mm Noncannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
5.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0422-2013·2012-11-28
King Systems Recalls Laryngeal Airway Devices Due to Sterilization Indicator Issues
King Systems Corp. is recalling specific lots of KING LAD Standard ClearSeal laryngeal airway devices because the ethylene oxide sterilization indicators did not change color as expected.
Product
KING LAD Standard ClearSeal SINGLE USE, King Systems ETO Sterilie10 devices/case Size 3 / Child ClearSeal King LAD¿ Patient Size: 30-50kg Product Usage: Laryngeal airway
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0381-2013·2012-11-28
Stryker Mantis Torque Wrench Recalled for Hex Tip Fracture
Stryker Spine is recalling 19 Mantis Torque Wrenches because the hex tip may fracture during use. The recall covers units distributed in the US and internationally.
Product
Stryker MANTIS TORQUE WRENCH REF 48287028 Manufactured by: Stryker pine SAS Z.I MARTICOT-33610-CESTAS-FRANCE +33 (0)5.57.97.06.30 http://www.stryker.com Distributed in the USA by: Stryker Spine, 2 Pearl Ct. Allendale NJ 07401-1677 USA +1-201-780-8000 The Xia…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0350-2013·2012-11-28
NuVasive Recalls 5.5mm Cannulated Screw Shank Due to Disengagement Risk
NuVasive Inc is recalling 240 units of 5.5mm x 35mm Cannulated Screw Shanks because the tulip portion can disengage from the shank after implantation.
Product
5.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0380-2013·2012-11-28
Stryker XIA 3 Torque Wrench Recalled Due to Hex Tip Fracture
Stryker Spine is recalling 54 XIA 3 Torque Wrenches because the hex tip may fracture during use, posing a risk of injury to patients or providers.
Product
Stryker XIA 3 TORQUE WRENCH REF 48237028 Manufactured by: Stryker pine SAS Z.I MARTICOT-33610-CESTAS-FRANCE +33 (0)5.57.97.06.30 http://www.stryker.com Distributed in the USA by: Stryker Spine, 2 Pearl Ct. Allendale NJ 07401-1677 USA +1-201-780-8000 The Xia…
Category
Medical Device
Distribution
Distributed nationwide

How to read this listing

Filters

27051–27075 of 27722