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. 2,467 recalls have been distributed to Alabama in the last 12 months.
Showing 24641–24660 of 28,641 recalls
Recalled Item: UPGRD PRGM 9734638 ADD AxiEM NAVIGATION Recalled by Medtronic Navigation,...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 6"x8" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Composix" LIP Mesh with Echo PS" 8"x10" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 4"x6" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 6"x10" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Composix" LP with Echo PS" 6 x8 Reorder Number: 0144680 Indicated Recalled...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿Ventralight" ST Mesh with Echo PS" 10"x13" Reorder Number: 5955113...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Composix" LP with Echo PS" 10x13 HUXH0294 HUXL0314 Indicated for Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Composix" LIP Mesh with Echo PS" 7"x9" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Amia Automated PD systems are used in the treatment Recalled by...
The Issue: System error 01779 is produced when the battery cannot be charged due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 12"x14" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 8"x10" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Composix" LP with Echo PS" 6x10 Reorder Number: 0144610 Indicated Recalled...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoswift¿ PGCL [poly (glycolide-co-caprolactone)] Absorbable Surgical...
The Issue: CP Medical, Inc., is recalling one lot of Monoswift PGCL [poly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) Recalled...
The Issue: Software issues with ACUSON SC2000 ultrasound with software version 3/5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) and...
The Issue: Potential malfunction due to a software issue for ACUSON SC2000 ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gluma Desensitizer Power Gel Product Usage: Usage: This is a Recalled by...
The Issue: The firm discovered that the Gluma Desensitizer Power Gel can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam camera system. Emission Computed Tomography System used to detect...
The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump model 8100 with software version 9.1.18 and software Recalled by...
The Issue: CareFusion is recalling the Alaris Pump model 8100 version 9.1.18 because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia E camera system. Emission Computed Tomography System used to Recalled...
The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.