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. 1,035 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,035 in last 12 months

Showing 35561–35580 of 53,623 recalls

FoodJuly 5, 2016· QualiTech, Inc

Recalled Item: FE Red Bell Pepper Recalled by QualiTech, Inc Due to Potential E. coli...

The Issue: QualiTech has been notified by a supplier that they received material with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2016· QualiTech, Inc

Recalled Item: FE Bacon 286 Recalled by QualiTech, Inc Due to Potential E. coli Contamination

The Issue: QualiTech has been notified by a supplier that they received material with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2016· QualiTech, Inc

Recalled Item: FE Spinach 352 Recalled by QualiTech, Inc Due to Potential E. coli Contamination

The Issue: QualiTech has been notified by a supplier that they received material with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2016· QualiTech, Inc

Recalled Item: FE Jalapeno 321A Recalled by QualiTech, Inc Due to Potential E. coli...

The Issue: QualiTech has been notified by a supplier that they received material with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2016· QualiTech, Inc

Recalled Item: FE Maple Recalled by QualiTech, Inc Due to Potential E. coli Contamination

The Issue: QualiTech has been notified by a supplier that they received material with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2016· QualiTech, Inc

Recalled Item: FE Carrot 281 Recalled by QualiTech, Inc Due to Potential E. coli Contamination

The Issue: QualiTech has been notified by a supplier that they received material with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2016· QualiTech, Inc

Recalled Item: PE Blueberry Recalled by QualiTech, Inc Due to Potential E. coli Contamination

The Issue: QualiTech has been notified by a supplier that they received material with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2016· QualiTech, Inc

Recalled Item: FE Rainbow Blend 714 Recalled by QualiTech, Inc Due to Potential E. coli...

The Issue: QualiTech has been notified by a supplier that they received material with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 5, 2016· QualiTech, Inc

Recalled Item: FE Jalapeno 709 Recalled by QualiTech, Inc Due to Potential E. coli...

The Issue: Quali Tech has been notified by a supplier that they received material with...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 5, 2016· Implant Direct Sybron Manufacturing, LLC

Recalled Item: RePlant¿ Angled Abutment Part Number 6050-52-60 Recalled by Implant Direct...

The Issue: Issue with design specification; oversized condition.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿ 500 v2.2.2A Software Upgrade Kit Recalled by Siemens...

The Issue: Some v2.2.2 upgrade kits include a dialysate mode which not cleared/approved...

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

Class III — Low RiskOngoing
Medical DeviceJuly 5, 2016· Branan Medical Corporation

Recalled Item: AmediCheck Instant Test Cup Recalled by Branan Medical Corporation Due to...

The Issue: Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug...

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

Class III — Low RiskOngoing
Medical DeviceJuly 5, 2016· The Binding Site Group, Ltd.

Recalled Item: Optilite Freelite Lambda Free Kit Product Code: LK018.OPT Recalled by The...

The Issue: Batch numbers listed are reporting Lambda Free Light Chain results >114mg/L...

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

Class II — Potential Health HazardOngoing
DrugJuly 5, 2016· Let's Talk Health, Inc.

Recalled Item: Oxygen Nasal Wash (purified water Recalled by Let's Talk Health, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: product is an unapproved drug due to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece w/o Hose Recalled by Zimmer Surgical Inc...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing