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. 2,520 recalls have been distributed to Alabama in the last 12 months.
Showing 20681–20700 of 50,591 recalls
Recalled Item: EVENCARE G3 Blood Glucose Test Strips Recalled by Medline Industries Inc Due...
The Issue: Incomplete seal and premature expiration of individually packaged Blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Behind-the-Ear hearing aids Recalled by GN Hearing A/S Due to GN Hearing...
The Issue: GN Hearing received reports from our manufacturing site in US regarding a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE TITANIUM NON- FILLED Recalled by Angiodynamics Inc....
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XCELA Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to Snap...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFLO 8F SINGLE PLASTIC NON-FILLED Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Snap lock connectors provided within implantable port kits may not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemo-Drop Blood Dispenser Recalled by Biomedical Polymers, Inc. Due to The...
The Issue: The metal cannula of the device either broke and the broken piece left in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual Diff Dropper Recalled by Biomedical Polymers, Inc. Due to The metal...
The Issue: The metal cannula of the device either broke and the broken piece left in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eversense CGM SENSOR (FG-4200-00-301)-Continuous Glucose Monitor Recalled by...
The Issue: Eversense Sensors have prematurely stopped functioning due to inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the Recalled by...
The Issue: Potential ability to leak once used for compounding.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydroclhoride Jelly USP Recalled by Akorn, Inc. Due to cGMP...
The Issue: cGMP Deviations: firm reported finding metal particulate matter in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SE Grocers **BAKERY** 18 CT Variety Pack Cookies Recalled by SOUTHEASTERN...
The Issue: 18 count Variety Pack cookies made in-store bakeries included Peanut Butter...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SE Grocers **BAKERY** 18 CT Peanut Butter Cookies Recalled by SOUTHEASTERN...
The Issue: 18 count Peanut Butter cookies made in-store bakeries failed to declare...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pneumothorax Tray Recalled by Cook Inc. Due to Lidstock perforation line may...
The Issue: Lidstock perforation line may be over the sterile area of the tray, when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gold Medal Enriched Recalled by General Mills, Inc Due to Potential E. coli...
The Issue: 5 lb. bags of Gold Medal Unbleached All Purpose flour have the potential to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IceCure Cryoablation System ProSense -Intended for cryogenic destruction of...
The Issue: Updated User Manual DSR3200000 Rev. E to include the safety guidelines in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KT RECOVERY+ ICE/HEAT MASSAGE BALL Rolling ball with hot and Recalled by KT...
The Issue: If over-heated may leak which, if not noticed, may cause hot fluid to come...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicrea Pass LP Trocar K-wire 01.6mm x 500mm-Nitinol Product Recalled by...
The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product : Recalled by...
The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.