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. 2,793 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,793 in last 12 months

Showing 1222112240 of 53,623 recalls

FoodJuly 13, 2022· Shopaax.com

Recalled Item: Kingdom Honey Royal Honey VIP The Ultimate Power Source Recalled by...

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 13, 2022· Paragon 28, Inc.

Recalled Item: Grappler Suture Anchor Recalled by Paragon 28, Inc. Due to Suture anchor may...

The Issue: Suture anchor may break upon insertion, which could lead to potential debris...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2022· Materialise USA LLC

Recalled Item: ProPlan CMF Anatomical Model Recalled by Materialise USA LLC Due to...

The Issue: MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· FUJIFILM Healthcare Americas Corporation

Recalled Item: Surpria 64: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...

The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· FUJIFILM Healthcare Americas Corporation

Recalled Item: SCENARIA View: Software Version V1.08 Recalled by FUJIFILM Healthcare...

The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· FUJIFILM Healthcare Americas Corporation

Recalled Item: Surpria: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...

The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Sensis or Sensis Vibe Combo systems as follows: System Recalled by...

The Issue: The Sensis Signal Input Box provides hooks as a milled item on the bottom of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
DrugJuly 11, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Tacrolimus Ointment Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Defective Container: Tube split from side seam

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

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Ativan Injection (lorazepam injection Recalled by Hikma Pharmaceuticals USA...

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
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

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
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

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
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Lorazepam Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to Failed...

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
Medical DeviceJuly 11, 2022· WISSNER-BOSSERHOFF GMBH

Recalled Item: SafeControl handset (a component of the Sentida bed which moves Recalled by...

The Issue: When the handset is disconnected from the power mains, and mains operation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2022· Synapse Biomedical Inc

Recalled Item: NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG)...

The Issue: Due to a defect identified on the EPG controller printed circuit board...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Due to a software...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam AXL Wave . Used to image the anterior segment of the eye. Recalled...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam HR . Used to image the anterior segment of the eye. Recalled by...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

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

Class II — Potential Health HazardOngoing