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.

50,591 total recalls
2,467 in last 12 months

Showing 2790127920 of 50,591 recalls

Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Recalled by Howmedica Osteonics Corp. Due to Revision rate identified...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Standard Extended Stem Recalled by Howmedica Osteonics Corp. Due to...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: Radio Capitellum Small Recalled by Howmedica Osteonics Corp. Due to Revision...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Recon Stem Implant 6mm Collar Recalled by Howmedica Osteonics Corp....

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Recalled by Howmedica Osteonics Corp. Due to Revision rate identified...

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Howmedica Osteonics Corp.

Recalled Item: rHead Recon Stem Implant Plasma Coated Recalled by Howmedica Osteonics Corp....

The Issue: Revision rate identified as higher than other proximal radial head...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee Spacer Blocks To assist in partial knee Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the Persona Partial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Medtronic Minimally Invasive Therapies Group

Recalled Item: Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is...

The Issue: Incorrect packaging. In one lot of Argyle Suction Tubing, the pouch may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Medacta Usa Inc

Recalled Item: The GMK knee system: designed for cemented use in total Recalled by Medacta...

The Issue: Medacta has observed a worldwide occurrence rate of post-operative insert...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2017· Radiometer America Inc

Recalled Item: ABL800 analyzer with FLEXQ module. Device intended for in vitro Recalled by...

The Issue: Due to misinterpretation of the barcode by the scanner, when the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2017· Medline Industries Inc

Recalled Item: Sensicare Green Surgical Glove Recalled by Medline Industries Inc Due to...

The Issue: Possible open seal on top portion of the package. Could cause breach of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodOctober 21, 2017· Tres Latin Foods

Recalled Item: Tres Latin Foods Kale & Pinto Bean pupusas Stuffed Corn Tortillas Recalled...

The Issue: Tres Latin Foods is recalling specific code dates of Kale & Pinto Bean 10...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 21, 2017· Tres Latin Foods

Recalled Item: Tres Latin Foods Pupusas Recalled by Tres Latin Foods Due to Undeclared Milk

The Issue: Tres Latin Foods is recalling specific code dates of Kale & Pinto Bean 10...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 20, 2017· Pfizer Inc.

Recalled Item: Zoloft (sertraline HCl) tablets 25 mg* 30-count bottle Recalled by Pfizer...

The Issue: SUPERPOTENT: Weight variations resulting in tablets that are sub and super...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2017· Pfizer Inc.

Recalled Item: diphenoxylate hydrochloride and atropine sulfate tablets Recalled by Pfizer...

The Issue: SUPERPOTENT: Weight variations resulting in tablets that are sub and super...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 20, 2017· Terumo BCT, Inc.

Recalled Item: HARVEST TERUMOBCT Recalled by Terumo BCT, Inc. Due to Certain lots of the...

The Issue: Certain lots of the Harvest Graft Delivery System GDP-10 Procedure Packs may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 19, 2017· Allergan Sales, LLC

Recalled Item: Combigan (brimonidine tartrate/timolol maleate ophthalmic solution)...

The Issue: Failed Impurities/Degradation Specifications.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 19, 2017· Allergan Sales, LLC

Recalled Item: Lumigan (bimatoprost ophthalmic solution) 0.01% Recalled by Allergan Sales,...

The Issue: Failed Impurities/Degradation Specifications.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: fentaNYL as citrate 2 mcg / mL Recalled by SCA Pharmaceuticals, LLC Due to...

The Issue: Lack Of Assurance Of Sterility.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: oxyTOCIN 30 units added to Lactated Ringers 500 mL Bag Recalled by SCA...

The Issue: Lack Of Assurance Of Sterility.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund