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. 1,056 recalls have been distributed to Alabama in the last 12 months.
Showing 16881–16900 of 50,591 recalls
Recalled Item: HRV Carrot.Cubes 1/20LB/HRV DCD Cartos 1/20LB - bag in box Recalled by...
The Issue: Products may contain metal fragments (foreign objects).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Mixed Veg (4) 12/32oz/GE Mixed Veg (4) 12/32oz - Recalled by Bonduelle...
The Issue: Products may contain metal fragments (foreign objects).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Succinylcholine Chloride PF Inj. 200 mg/10 mL Recalled by US Compounding Inc...
The Issue: Labeling: Incorrect or Missing lot and/or expiration date: The lot number...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Penumbra JET 7 Reperfusion Catheter The Penumbra JET Recalled by Penumbra...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7MAX KIT Penumbra JET 7 Reperfusion Catheter+ MAX Recalled by...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUITY Universal Cutter Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific (BSC) is retrieving five Model 7060 ACUITY cutters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WAHL 4212 HEATED MASSAGER Recalled by Wahl Clipper Corp Due to The...
The Issue: The connection between the massager and heat element can overheat causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products TP Slides- IVD measure total protein (TP) Recalled...
The Issue: Eltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORTEX Bivona Cuffless Neonatal/Pediatric FlexTend Tracheostomy Tube...
The Issue: A specific model and lot number of Bivona Cuffless FlexTend Tracheostomy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT Chemistry Products ALB-TP Slides (ALB is not affected) Recalled by...
The Issue: Eltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle Cups Recalled by DePuy Orthopaedics, Inc. Due to Certain Pinnacle...
The Issue: Certain Pinnacle Cup devices may potentially exhibit an oversized "minor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EliA dsDNA Well - Product Usage: intended for the In-Vitro Recalled by...
The Issue: Decreased values for EliA ANA Positive Control when using the EliA dsDNA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENOVO Venous Stent System 9F Product Description(REF)/dimension: VENEL14040...
The Issue: Reports of the proximal end of the stent not immediately expanding upon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENOVO Venous Stent System 8F Product Description(REF)/dimension: VENEL10040...
The Issue: Reports of the proximal end of the stent not immediately expanding upon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENOVO Venous Stent System 10F Product Description(REF)/dimension:...
The Issue: Reports of the proximal end of the stent not immediately expanding upon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bactiseal Ventricular Catheter with Bactiseal Shunt System - Product Usage:...
The Issue: Mislabeled product-Bactiseal Ventricular Catheter with Bactiseal Shunt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRYTIME MEDICAL REBOA Catheter Introducer Kit Recalled by Prytime Medical...
The Issue: There is a potential that a catheter convenience set contains a 21G access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bactiseal Endoscopic Ventricular Catheter: EVC- Catheter is designed for use...
The Issue: Mislabeled product-Bactiseal Ventricular Catheter with Bactiseal Shunt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.