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. 2,748 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,748 in last 12 months

Showing 1726117280 of 53,623 recalls

DrugMarch 15, 2021· Cardinal Health Inc.

Recalled Item: Namzaric (memantine HCl extended release and donepezil HCl) capsules 14...

The Issue: CGMP Deviations: Intermittent exposure to temperature excursion during storage.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 15, 2021· Nuts.com

Recalled Item: Nuts.com brand Diced Dried Figs packaged in 1lb stand up gusset pouches....

The Issue: Undeclared almonds in diced fig product

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 15, 2021· Medtronic Minimed

Recalled Item: MiniMed 670G Insulin Pump: Models: PUMP MMT-1740KX 670G V6.3 SF MG CLIN...

The Issue: Due to a software design issue, under certain conditions, a software fault...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2021· Medtronic Minimed

Recalled Item: MiniMed 780G Insulin Pump: Models: PUMP MMT-1885 MM780G 6.5V BLE MMOL...

The Issue: Due to a software design issue, under certain conditions, a software fault...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2021· St. Jude Medical, Cardian Rhythm Management Division

Recalled Item: ENDURITY Pulse Generator **** SN ********* St. Jude Medical Recalled by St....

The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2021· St. Jude Medical, Cardian Rhythm Management Division

Recalled Item: ASSURITY Pulse Generator **** SN ********* ST. JUDE MEDICAL Recalled by St....

The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2021· B. Braun Medical, Inc.

Recalled Item: Filtered Triple-Leg Extension Set - Intravascular administration set....

The Issue: BBMI has identified through complaints the potential for the extension set...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2021· Medline Industries Inc

Recalled Item: Diluent Recalled by Medline Industries Inc Due to Possible false negative or...

The Issue: Possible false negative or false positive results due to the product being...

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2021· Ferring Pharmaceuticals Inc

Recalled Item: ZOMA-Jet 10 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...

The Issue: Defective Delivery System: customer complaints concerning the injector pen...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2021· Ferring Pharmaceuticals Inc

Recalled Item: ZOMA-Jet 5 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...

The Issue: Defective Delivery System: customer complaints concerning the injector pen...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2021· Breckenridge Pharmaceutical, Inc

Recalled Item: Omeprazole Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2021· Sagent Pharmaceuticals Inc

Recalled Item: Phenylephrine HCl Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Lack of Assurance of Sterility: customer complaints of loose crimped vial...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2021· LIEBEL-FLARSHEIM COMPANY LLC

Recalled Item: HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW)...

The Issue: Failure to comply with the performance standard for fluoroscopy systems. Per...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2021· Krishe Inc

Recalled Item: Dasky Disposable Sampling Tube Recalled by Krishe Inc Due to Verification...

The Issue: Verification and validation of the virus transport medium tubes was not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2021· Stryker Spine

Recalled Item: Tritanium X TL Instruments - intervertebral fusion device with bone graft...

The Issue: Stryker identified non-conforming instruments that are components of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2021· Krishe Inc

Recalled Item: Disposable Sampling Tube Recalled by Krishe Inc Due to Verification and...

The Issue: Verification and validation of the virus transport medium tubes was not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2021· Krishe Inc

Recalled Item: Dasky Disposable Sampling Tube Recalled by Krishe Inc Due to Verification...

The Issue: Verification and validation of the virus transport medium tubes was not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2021· Krishe Inc

Recalled Item: Dasky Disposable Sampling Tube Recalled by Krishe Inc Due to Verification...

The Issue: Verification and validation of the virus transport medium tubes was not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2021· Arthrex, Inc.

Recalled Item: Tibial Opening Wedge Osteotomy Plate Recalled by Arthrex, Inc. Due to It was...

The Issue: It was discovered that five AR-13200ST-15.0 parts were processed as...

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

Class II — Potential Health HazardOngoing
DrugMarch 10, 2021· China Gel Inc

Recalled Item: CHINA-GEL WHITE (Camphor 3.00% Recalled by China Gel Inc Due to CGMP...

The Issue: CGMP deviations: Product being recalled as it was made in the same facility...

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

Class II — Potential Health HazardOngoing
Refund