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. 2,786 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,786 in last 12 months

Showing 1418114200 of 53,623 recalls

Medical DeviceJanuary 20, 2022· Ventana Medical Systems Inc

Recalled Item: BenchMark ULTRA and DISCOVERY ULTRA Instruments Recalled by Ventana Medical...

The Issue: Potential for Fluid Leak inside a staining system that could cause an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Outset Medical, Inc.

Recalled Item: Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000...

The Issue: Due to a component in the hemodialysis console there is the possibility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5 Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: SAFE-T PLUS ATRAUMATIC ADULT LP TRAY Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE DRUG FREE TRAY 22G Recalled by Bard Peripheral Vascular Inc...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY ADULT 18G X 3.5 Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: ADULT LUMBAR PUNCTURE DRUG FREE TRAY 20G Recalled by Bard Peripheral...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: SAFE-T PLUS LUMBARPUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP Recalled by Bard Peripheral Vascular...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL Recalled by Bard Peripheral...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Bard Peripheral Vascular Inc

Recalled Item: Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray Recalled by Bard...

The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2022· Envisiontec US Llc

Recalled Item: PCA 4000 Curing Units Recalled by Envisiontec US Llc Due to The PCA 4000 may...

The Issue: The PCA 4000 may not fully cure EnvisionTEC dental resins to desired product...

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

Class II — Potential Health HazardOngoing
DrugJanuary 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed stability specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed stability specifications

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

Class III — Low RiskOngoing
Refund
DrugJanuary 19, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Bortezomib Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed stability specifications

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

Class III — Low RiskOngoing
Refund
FoodJanuary 19, 2022· Frozen Food Development Inc

Recalled Item: Steamable by Lidl Chopped Spinach NET WT 12 OZ (340 Recalled by Frozen Food...

The Issue: Possible contamination of Listeria monocytogenes in frozen chopped spinach.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 19, 2022· Amys Kitchen Inc

Recalled Item: Amy's Vegan Organic Rice Mac & Cheese Recalled by Amys Kitchen Inc Due to...

The Issue: Firm investigation detected trace amounts of milk through finished product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 19, 2022· Volcano Corporation

Recalled Item: SyncVision Systems Recalled by Volcano Corporation Due to If FFR...

The Issue: If FFR measurement(s) are made prior to an iFR/FFR co-registration/pullback...

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

Class II — Potential Health HazardOngoing