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 20581–20600 of 50,591 recalls
Recalled Item: 2.4mm x 2.5 Fluted Pin Pouch Recalled by Exactech, Inc. Due to Potential for...
The Issue: Potential for the 2.4mm x 2.5 Fluted Pin Pouch to contain a single pin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCFE (slipped capital femoral epiphysis) Knobs for Driver Recalled by Pega...
The Issue: There is a potential for the screws to have become loosened during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection Recalled...
The Issue: Lack of Assurance of Sterility: Bag has the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zentrip (meclizine Hydrochloride) Recalled by Sato Pharmaceutical Inc. Due...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Motion Sickness (meclizine hydrochloride) 25 mg tablets Recalled by Sato...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sankaijo BOTANICAL LAXATIVE (docusate sodium 8.33 mg and sennosides 1.36...
The Issue: Subpotent Drug: Formulated amount of sennosides component is less than...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WAL-DRAM 2 (meclizine Hydrochloride) 25 mg tablets Recalled by Sato...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Motion Sickness Strips (meclizine hydrochloride) 25 mg strips Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 Recalled by...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rosie4 Vital Signs Monitor with NIBP valve assembly board Recalled by...
The Issue: NIBP valve assembly board subject to this recall includes enhancements that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs Recalled...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Groshong 9.5 Dual-Lumen CV Catheter Recalled by Bard Peripheral Vascular...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Recalled by...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rosebud Vital Signs Monitor with NIBP valve assembly board Recalled by...
The Issue: NIBP valve assembly board subject to this recall includes enhancements that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. X-Port isp M.R.I Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.