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. 1,073 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,073 in last 12 months

Showing 24601–24620 of 53,623 recalls

DrugMarch 7, 2019· Medtech Products, Inc.

Recalled Item: Little Remedies New Baby Essentials Kit. Each kit contains 1 Recalled by...

The Issue: Incorrect/undeclared excipients: Kit carton bear incorrect labeling for two...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2019· American Health Packaging

Recalled Item: Valsartan Tablets USP 160 mg Recalled by American Health Packaging Due to...

The Issue: CGMP Deviation: Presence of NDEA (N-Nitrosodimethylamine), a carcinogen...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Docetaxel Injection USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Defective Container: complaint for seal and cap vial issues that could lead...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 6, 2019· Topcon Medical Systems, Inc.

Recalled Item: IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a Recalled by Topcon...

The Issue: When a patient is selected in the patient data and another patient is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2019· BioFire Diagnostics, LLC

Recalled Item: FilmArray Gastrointestinal (GI) Panel Recalled by BioFire Diagnostics, LLC...

The Issue: Elevated rates of false positive results for Campylobacter and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2019· PROCEPT BIOROBOTICS CORPORATION

Recalled Item: AquaBeam Handpiece Recalled by PROCEPT BIOROBOTICS CORPORATION Due to...

The Issue: Certain lots may develop an internal leak due to a micro-crack in a specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2019· Fenwal Inc

Recalled Item: Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled...

The Issue: Based on internal investigations, Fresenius Kabi has identified a...

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

Class II — Potential Health HazardOngoing
DrugMarch 5, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by AVKARE Inc....

The Issue: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium Tablets USP 50 mg 50 Tablets (5x10) Unit Dose boxes...

The Issue: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2019· USA LESS Inc.

Recalled Item: LEOPARD Miracle Honey packaged in a wooden box Recalled by USA LESS Inc. Due...

The Issue: Marketed Without An Approved NDA/ANDA: product tainted with undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 5, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by AVKARE Inc....

The Issue: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2019· Petra Hygienic Systems Int Ltd

Recalled Item: ATHLETICARE Anti-Bacterial Hand Soap AC 550 (triclosan) Recalled by Petra...

The Issue: Does Not Meet Monograph: product contains, triclosan, an ingredient that can...

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

Class III — Low RiskOngoing
Refund
FoodMarch 4, 2019· Procesadora Aguas Claras LTDA.

Recalled Item: Premium Sustainable Atlantic Salmon (Farm Raised) Recalled by Procesadora...

The Issue: Direct customer tested Premium Sustainable Atlantic Salmon (Farm Raised)...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 1, 2019· Lamb Weston Inc

Recalled Item: Lamb's Supreme Starz Recalled by Lamb Weston Inc Due to Foreign Object...

The Issue: Lamb's Supreme Starz (Star-shaped Hash Brown Patties) are recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 1, 2019· Integra Limited

Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...

The Issue: Temperature indicator may have changed color to dark gray or black prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2019· Medical Action Industries Inc

Recalled Item: Laparotomy Sponge with the following product description and model numbers:...

The Issue: Potential lack of sterility assurance

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx30mm-Low Profile...

The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet RingLoc Hip System Self-Tapping Bone Screw 6.5mmx20mm-Low Profile...

The Issue: Two lengths of the 6.5mm RingLoc Hip System Self-Tapping Bone Screw may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2019· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 Coring Tool Recalled by Thoratec Corp. Due to Small...

The Issue: Small black plastic particle was observed in the left ventricle during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2019· Integra Limited

Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...

The Issue: Temperature indicator may have changed color to dark gray or black prior to...

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

Class II — Potential Health HazardOngoing