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 27761–27780 of 50,591 recalls
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClariVein IC infusion catheter Recalled by Vascular Insights, LLC Due to...
The Issue: Certain catheters could have a compromised catheter shaft due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista System LOCI 8 CALIBRATOR The LOCI 8 Calibrator Recalled by...
The Issue: An increase in the number of failed calibration events or negative bias with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liothyronine Sodium Tablets Recalled by Mayne Pharma Inc Due to Failed...
The Issue: Failed Dissolution Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GERICARE Eyewash Recalled by Kareway Products Inc Due to Non-sterility:...
The Issue: Non-sterility: confirmed microbial contamination with Achromobacter xylosoxidans
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clozapine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Tablet/Capsule Specifications; potential presence of broken tablets.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dark Chocolate covered Gingersnaps. Packaged as follows: 1. in clear...
The Issue: Figi's is recalling Gift #0368 Christmas Gingersnap Variety and Bulk Dark...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Maximum Strength Zephrex-D Recalled by L. Perrigo Company Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medivance(R) ARCTIC SUN(R) ARCTICGEL(TM) Pads: Description Recalled by Bard...
The Issue: Specific lots of ArcticGel Pads have potential issues which may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...
The Issue: Superpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...
The Issue: Device may potentially be compromised by water in end user packaging....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...
The Issue: Device may potentially be compromised by water in end user packaging....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...
The Issue: Stent possibly unable to be fully released from the delivery system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...
The Issue: Stent possibly unable to be fully released from the delivery system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden Classic 55 Toric Daily Wear Soft contact Recalled by Alden Optical Due...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver Xstar Safety Crescent Recalled by Beaver-Visitec International...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everflex Self-Expanding Peripheral Stent with Entrust Delivery System...
The Issue: Stent length on the label may not match the length of the stent itself.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaKone Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.