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. 2,478 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,478 in last 12 months

Showing 2644126460 of 50,591 recalls

FoodApril 24, 2018· Labrada Nutrition, Inc

Recalled Item: Lean Pro 8 Cookies & Cream 1 Recalled by Labrada Nutrition, Inc Due to...

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 24, 2018· Labrada Nutrition, Inc

Recalled Item: Lean Pro 8 Vanilla 2 Recalled by Labrada Nutrition, Inc Due to Undeclared Egg

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(R) STERILE R Recalled by Medline Industries Inc Due...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2018· Medline Industries Inc

Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...

The Issue: The product packaging seal has the potential to experience seal creep. This...

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

Class II — Potential Health HazardOngoing
DrugApril 23, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Dr. Reddy's...

The Issue: Presence of Foreign Tablets/Capsules: One foreign tablet identified as...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2018· Mckesson Packaging Services

Recalled Item: Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules Recalled by...

The Issue: Failed Dissolution Specifications. High dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugApril 23, 2018· Mckesson Packaging Services

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mckesson Packaging...

The Issue: Failed Dissolution Specifications. High dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugApril 23, 2018· Mckesson Packaging Services

Recalled Item: Diltiazem HCl Extended-Release Capsules Recalled by Mckesson Packaging...

The Issue: Failed Dissolution Specifications. High dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 23, 2018· Tandem Diabetes Care Inc

Recalled Item: t:slim G4 Insulin Pump with Dexcom G4 Platinum CGM Software version: 4.3.4.3...

The Issue: The fuel gauge, the component that reads and reports the battery parameters...

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

Class II — Potential Health HazardOngoing
DrugApril 20, 2018· Exela Pharma Sciences LLC

Recalled Item: Diclofenac Sodium and Misoprostol Delayed Release Tablets 75 mg/0.2 mg...

The Issue: Labeling: Label Mix-Up: bottle labeled as Diclofenac Sodium and Misoprostol...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 20, 2018· CareFusion 303, Inc.

Recalled Item: Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris...

The Issue: Complaints where users were unable to prime the administration set.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Go.Up Recalled by Siemens Medical Solutions USA, Inc Due to There is...

The Issue: There is a potential for a software issue that may cause the need for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to There...

The Issue: There is a potential for a software issue that may cause the need for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

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

Class II — Potential Health HazardOngoing