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.
Showing 4801–4820 of 28,641 recalls
Recalled Item: Water Filter MAJ-2318. This MAJ-2318 water filter has been designed Recalled...
The Issue: Water filter may have been assembled incorrectly, resulting in unfiltered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IV Start Kit Recalled by Medical Action Industries, Inc. 306 Due to The kits...
The Issue: The kits contain saline flush syringes which were recalled by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)...
The Issue: When using those products you may experience difficulties to extend or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible Recalled...
The Issue: European version of microcatheter were distributed within US which contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible Recalled...
The Issue: European version of microcatheter were distributed within US which contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...
The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brasseler 8S RA SHP RD (Super-Sharp Round) H1S.21.023 Recalled by Brasseler...
The Issue: The device has a grip detail (right angle latch) out of specification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.2.100 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synapse PACS - Version 7.1.000 Recalled by FUJIFILM Healthcare Americas...
The Issue: Measurements on a Secondary Capture 2D image, that does not have pixel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.