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. 2,753 recalls have been distributed to Georgia in the last 12 months.
Showing 15301–15320 of 53,623 recalls
Recalled Item: MENTOR Saline-Filled Breast Implants are constructed from room temperature...
The Issue: Due to a manufacturing issue, Implant may have a potentially weakened area...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tone s Taco Seasoning Blend Recalled by B&G Foods North America, Inc Due to...
The Issue: Product was recalled due to the presence of undeclared wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARCHITECT i1000SR /1L86 and 1L87 Recalled by Abbott Laboratories Due to...
The Issue: Twelve software-related issues affecting software version 9.41 and earlier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 /2P24 Recalled by Abbott Laboratories Due to Twelve...
The Issue: Twelve software-related issues affecting software version 9.41 and earlier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Generator 220V Cooper Surgical Part Number: LP-20-220...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Generator 120V Cooper Surgical Part Number: LP-20-120...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodialysis Delivery System Recalled by Baxter Healthcare Corporation Due...
The Issue: If the operator initiates therapy with a saved prescription profile and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Natural Dentist Healthy Balance Peppermint Sage Recalled by Revive...
The Issue: Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...
The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...
The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flexor Check-Flo Introducer - Raabe Modification Recalled by Cook Inc. Due...
The Issue: Affected lots may be manufactured incorrectly with the radiopaque marker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to Affected lots may...
The Issue: Affected lots may be manufactured incorrectly with the radiopaque marker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Tablets Recalled by Strides Pharma Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.