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 2820128220 of 50,591 recalls

Medical DeviceSeptember 14, 2017· C.R. Bard, Inc.

Recalled Item: Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box Recalled by...

The Issue: Several instances of a catheter caught in the sterile barrier seal and in...

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

Class II — Potential Health HazardOngoing
FoodSeptember 14, 2017· Shawnee Milling Company, Inc.

Recalled Item: Shawnee Mills Peppered Gravy Mix Recalled by Shawnee Milling Company, Inc....

The Issue: Potential for foreign material in a food product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 13, 2017· Zimmer Biomet, Inc.

Recalled Item: 979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument....

The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2017· Zimmer Biomet, Inc.

Recalled Item: 14-442000S Antegrade Femoral Nail Instrument Kit Recalled by Zimmer Biomet,...

The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2017· Zimmer Biomet, Inc.

Recalled Item: Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa Recalled by...

The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...

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

Class II — Potential Health HazardOngoing
DrugSeptember 13, 2017· Amgen, Inc.

Recalled Item: Procrit (epoetin alfa) Recalled by Amgen, Inc. Due to Presence of...

The Issue: Presence of particulate matter: glass flakes identified as lamellae observed...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2017· Vi-Jon, Inc.

Recalled Item: Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 Recalled by...

The Issue: Failed Stability Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 12, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim DRG Implantable Pulse Generator Model 3664 Recalled by St. Jude...

The Issue: Analysis of the difference between the actual device longevity and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2017· St. Jude Medical, Inc.

Recalled Item: Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse...

The Issue: Analysis of the difference between the actual device longevity and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2017· St. Jude Medical, Inc.

Recalled Item: Proclaim 5 Elite Implantable Pulse Generator and Proclaim 7 Elite Recalled...

The Issue: Analysis of the difference between the actual device longevity and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2017· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Medical Kalare Fluoroscopic X-Ray System (DREX-KL80) Kalare is...

The Issue: During an examination images were displayed on the live monitor,but the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2017· Abbott Point Of Care Inc.

Recalled Item: i-STAT DE handheld data processing module for clinical use Recalled by...

The Issue: Issues resulting from upgrade to software version 2.8: (1) Location,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2017· Zoll Manufacturing Corp.

Recalled Item: LifeVest Wearable Defibrillator Model 4000 Recalled by Zoll Manufacturing...

The Issue: Incorrect service code for properly catching critical defects during...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2017· Sysmex America, Inc.

Recalled Item: Sysmex Fluorocell(R) PLT Fluorocell PLT is used to stain platelets Recalled...

The Issue: There is potential that fluorescent platelet (PLT-F) and immature platelet...

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

Class II — Potential Health HazardOngoing
FoodSeptember 8, 2017· Apple King, LLC

Recalled Item: Fuji apples Recalled by Apple King, LLC Due to Fuji apples are recalled...

The Issue: Fuji apples are recalled because Thiabendazole was detected at 6.9 ppm.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 7, 2017· Garden Of Life, LLC

Recalled Item: Garden of Life Recalled by Garden Of Life, LLC Due to The product may pose a...

The Issue: The product may pose a choking hazard to newborns due to the thickness of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 7, 2017· Radiometer America Inc

Recalled Item: AutoCheck5+ Recalled by Radiometer America Inc Due to Radiometer has...

The Issue: Radiometer has recently become aware that a few of the AUTOCHECK 5+ level 2...

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

Class II — Potential Health HazardOngoing
FoodSeptember 5, 2017· NOW Foods

Recalled Item: Organic Coconut Sugar Recalled by NOW Foods Due to Undeclared Gluten

The Issue: Undeclared gluten found in the product and the product is labeled "Gluten Free".

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 5, 2017· Teva Pharmaceuticals USA

Recalled Item: Acarbose Tablets Recalled by Teva Pharmaceuticals USA Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: An incorrect expiration...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 5, 2017· Genentech, Inc.

Recalled Item: Activase (alteplase) Recalled by Genentech, Inc. Due to...

The Issue: Non-Sterility:presence of cracked or chipped glass at the neck of Sterile...

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

Class I — Serious Health HazardOngoing
Refund