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. 1,096 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
1,096 in last 12 months

Showing 16921–16940 of 53,623 recalls

Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10 G Coxaxial Cannula with Tuohy Connection Recalled by Zavation Due to...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL) Recalled by...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10G BEVELED TROCAR/CANNULA. For use in Orthopedic / spinal procedures....

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: CEMIX - CEMENT MIXING SYSTEM STERILE Recalled by Zavation Due to Products...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Cement Delivery Cannula Recalled by Zavation Due to Products...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Recalled by Zavation Due to Products distributed as sterile may not...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Biopsy Device Recalled by Zavation Due to Products distributed as...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Bard Peripheral Vascular Inc

Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...

The Issue: Catheters may experience difficulty in flushing, infusion, and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Bard Peripheral Vascular Inc

Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...

The Issue: Catheters may experience difficulty in flushing, infusion, and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Bard Peripheral Vascular Inc

Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...

The Issue: Catheters may experience difficulty in flushing, infusion, and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Roche Molecular Systems, Inc.

Recalled Item: cobas Liat Analyzer: respiratory virus panel nucleic acid assay system...

The Issue: Invalid or false positive results for one or more targets...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Roche Molecular Systems, Inc.

Recalled Item: cobas SARS-CoV-2 & Influenza A/B assay cobas Liat- Reagents Recalled by...

The Issue: Invalid or false positive results for one or more targets...

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2021· Namoo Enterprise LLC

Recalled Item: PremierZen Black 5000 capsules Recalled by Namoo Enterprise LLC Due to...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2021· S & B Story LLC

Recalled Item: Imperial Extreme 2000 Capsules Recalled by S & B Story LLC Due to Marketed...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2021· Cosette Pharmaceuticals, Inc.

Recalled Item: Mometasone Furoate Topical Solution Recalled by Cosette Pharmaceuticals,...

The Issue: CGMP Deviaitons

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Metformin HCl Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Moisture Limits: Out of specification for water content

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

Class III — Low RiskOngoing
Refund
DrugMarch 24, 2021· Bit & Bet LLC

Recalled Item: Thumbs Up 7 Blue 69K Recalled by Bit & Bet LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 24, 2021· Becton Dickinson & Co.

Recalled Item: BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended Recalled...

The Issue: BioGX SARS-CoV-2 Reagents for BD MAX" System rehydration buffer tubes were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2021· Gf Health Products

Recalled Item: Drop Arm Versamode" Recalled by Gf Health Products Due to The front casters...

The Issue: The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2021· Pacific Medical Group Inc.

Recalled Item: Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel Recalled by...

The Issue: Aftermarket front bezel components were installed during service/repair, not...

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

Class I — Serious Health HazardOngoing