Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,660 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,660 in last 12 months

Showing 52415260 of 28,641 recalls

Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 6-7-8. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for endoscopic...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 18-19-20. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 6-7-8. indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 11-12-13. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 8.5-9.5-10.5. indicated for endoscopic dilation...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 8.5-9.5-10.5. Indicated for endoscopic dilation...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 11-12-13. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: Medex 700PSI STOPCOCK W/ROTATOR Recalled by Smiths Medical Asd Inc Due to...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: 20IN (50.8CM) BRAIDED INJ LINE Recalled by Smiths Medical Asd Inc Due to...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: Medex LOGICAL CATH LAB KIT Recalled by Smiths Medical Asd Inc Due to There...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 16-17-18. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: HIGH PRESSURE ROTATOR WITH FEMALE LUER LOCK Recalled by Smiths Medical Asd...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet Hanaulux HLX3000 OR Light Systems Recalled by Getinge Usa Sales Inc...

The Issue: A potential for a light system to fall in the operating room.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet Orchide OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...

The Issue: A potential for a light system to fall in the operating room.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Bard Peripheral Vascular Inc

Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/...

The Issue: The internal diameter of the coaxial cannula may be smaller or larger than...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet Rolite OR Light Systems Recalled by Getinge Usa Sales Inc Due to A...

The Issue: A potential for a light system to fall in the operating room.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet Lucea - Lucea10/40 Recalled by Getinge Usa Sales Inc Due to A...

The Issue: A potential for a light system to fall in the operating room.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2023· Getinge Usa Sales Inc

Recalled Item: Maquet PowerLEDII OR Light System Recalled by Getinge Usa Sales Inc Due to A...

The Issue: A potential for a light system to fall in the operating room.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing