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. 2,656 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,656 in last 12 months

Showing 2606126080 of 53,623 recalls

Medical DeviceSeptember 6, 2018· Stihler Electronic Gmbh

Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...

The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2018· Stihler Electronic Gmbh

Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...

The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2018· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Implant Direct Scan Adapter Assembly Replant platform for the following...

The Issue: The action is being initiated due to incorrect assembly of the scan adapter...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2018· BioFire Diagnostics, LLC

Recalled Item: FilmArray Blood Culture Identification (BCID) Recalled by BioFire...

The Issue: Increased risk of false positive results for Proteus when the product is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2018· Cordis Corporation

Recalled Item: Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is Recalled by...

The Issue: Product may not meet the internal manufacturing shaft subassembly burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2018· Thoratec Switzerland GMBH

Recalled Item: Thoratec CentriMag Motor Recalled by Thoratec Switzerland GMBH Due to...

The Issue: Reports of circulatory support system motor stopping. Motor stop can be...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· CooperSurgical, Inc.

Recalled Item: Colpo-Pneumo Occluder Recalled by CooperSurgical, Inc. Due to The seal of...

The Issue: The seal of the sterile pouch may be compromised, thereby increasing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· CooperSurgical, Inc.

Recalled Item: Retractor System Elastic Stays (Part 3314-lG Recalled by CooperSurgical,...

The Issue: There is a possibility that the seal of the sterile pouch may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· Alpha Omega Engineering

Recalled Item: Neuro Omega System Recalled by Alpha Omega Engineering Due to If cables are...

The Issue: If cables are improperly connected, current may reach high charge density,...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 4, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Vereos PET/CT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Software Correction: Software errors that may result in incorrect 4D CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· Cypress Medical Products LLC

Recalled Item: McKesson Insulin Syringe 0.3mL 31GX5/16 Item Numbers: 102-SN310C31516P...

The Issue: Small hole at the end of the syringe is impeding suction of liquid.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Hemotherm 400CE Recalled by Cincinnati Sub-Zero Products LLC, a Gentherm...

The Issue: Potential for membrane (control panel) switch errors leading to an inability...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· GE Healthcare Finland Oy

Recalled Item: GE Healthcare CARESCAPE Monitor B850 Product Usage: Intended uses of...

The Issue: When multiple CARESCAPEMonitor B450 or B850 units are connected to the same...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2018· GE Healthcare Finland Oy

Recalled Item: GE Healthcare CARESCAPE Monitor B450 Product Usage: Intended uses of...

The Issue: When multiple CARESCAPEMonitor B450 or B850 units are connected to the same...

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

Class II — Potential Health HazardOngoing
DrugSeptember 4, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Tizanidine HCl Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Presence of Foreign Tablets/Capsules: Glimepiride tablet was found in a...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2018· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Synjardy (empagliflozin and metformin hydrochloride) Tablets. 5 mg/1000 mg....

The Issue: Cross Contamination With Other Products:

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Muscle & Joint Pain Relief Homeopathic Formula Recalled by Beaumont Bio-med,...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Allergy & Hay Fever Relief Homeopathic Formula Recalled by Beaumont Bio-med,...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Sinus Response Homeopathic Formula Recalled by Beaumont Bio-med, Inc. Due to...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 31, 2018· Beaumont Bio-med, Inc.

Recalled Item: Skin Irritation & Itch Response Homeopathic Formula Recalled by Beaumont...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund