Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,686 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,686 in last 12 months

Showing 2012120140 of 53,623 recalls

DrugMarch 18, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Acetaminophen and Codeine Phosphate Tablets Recalled by Aurobindo Pharma USA...

The Issue: CGMP Deviations: Products were manufactured in a processing area in which...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 18, 2020· Lindt & Sprungli (USA), Inc.

Recalled Item: Lindt & Sprungli (USA) Recalled by Lindt & Sprungli (USA), Inc. Due to...

The Issue: Chocolate contains undeclared milk and soy

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: X12+ and patient cable for the X12+ Telemeter with the Recalled by WELCH...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Lead diagnostic electrocardiograph under the following device names: ELI 10...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor Recalled...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Replaceable lead set for the Wireless Acquisition Module (WAM) Recalled by...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: T12. Incorporates wireless electrocardiographic technology to achieve the...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Q-Tel. The Q-Tel RMS system is a computer-based cardiac and Recalled by...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: ELI PC. The ELI PC Service automatically converts resting ECG Recalled by...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: S4 and patient cable for the S4 Wireless Telemeter with Recalled by WELCH...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: H12+ and patient cable for the H12+ Holter Recorders with Recalled by WELCH...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Radiometer Medical ApS

Recalled Item: safeCLINITUBES Blood Sampler Recalled by Radiometer Medical ApS Due to The...

The Issue: The SafeCLINITUBES blood sampler may have insufficient aspiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Radiometer Medical ApS

Recalled Item: safeCLINITUBES Blood Sampler Recalled by Radiometer Medical ApS Due to The...

The Issue: The SafeCLINITUBES blood sampler may have insufficient aspiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Radiometer Medical ApS

Recalled Item: safeCLINITUBES Blood Sampler Recalled by Radiometer Medical ApS Due to The...

The Issue: The SafeCLINITUBES blood sampler may have insufficient aspiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: DR. THAMES - LAP CHOLE Recalled by Applied Medical Resources Corp Due to...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Clip Applier Kit Recalled by Applied Medical Resources Corp Due to There may...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Epix latis GRASPER Recalled by Applied Medical Resources Corp Due to There...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Applied Medical Resources Corp

Recalled Item: Epix latis GRASPER Recalled by Applied Medical Resources Corp Due to There...

The Issue: There may be a slightly protruding rivet on the distal end of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Becton Dickinson & Company

Recalled Item: PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge Recalled by...

The Issue: Iincorrectly packaged without the required lidocaine as labeled

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

Class II — Potential Health HazardOngoing