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. 2,858 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,858 in last 12 months

Showing 29813000 of 29,505 recalls

Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/4X3 Model/Catalog Number: 801398. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 3-1/2X6 Model/Catalog Number:801457. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/2X1 Model/Catalog Number: 801402. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 1X6-200 Model/Catalog Number: 801453. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: MICR PATIE RND Model/Catalog Number: 801396. CODMAN Surgical Patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/4X1-1/2 Model/Catalog Number: 801397. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/2X3 Model/Catalog Number: 801407. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 1/4X6 Model/Catalog Number: 801450. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1X1 Model/Catalog Number: 801403. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Covidien LP

Recalled Item: Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm Recalled by...

The Issue: Specific lots of the Chameleon PTA Balloon Catheter failed to meet in-house...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product...

The Issue: To better define the drying procedures described in the IFU to improve the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Medtronic Neuromodulation

Recalled Item: Medtronic Recharger Kits Recalled by Medtronic Neuromodulation Due to The...

The Issue: The Wireless Rechargers in the kits may be unable to enter a recharging...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Nihon Kohden America Inc

Recalled Item: Nihon Kohden Adult Ear Clip SpO2 Sensor Recalled by Nihon Kohden America Inc...

The Issue: Due to oximeters not having FDA market approval or clearance to distribute...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Nihon Kohden America Inc

Recalled Item: Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor Recalled by...

The Issue: Due to oximeters not having FDA market approval or clearance to distribute...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Baxter Healthcare Corporation

Recalled Item: a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed Recalled by Baxter...

The Issue: The beds have a potential for an interface issue with the Rauland Responder...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Polymer Technology Systems, Inc. dba PTS Diagnostics, Inc.

Recalled Item: A1CNow+ Multi-Test HbA1c System consists of (1) a semi-disposable...

The Issue: The reason for this recall is PTS Diagnostics, Inc. received complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2024· MicroSurgical Technology Inc

Recalled Item: Brand Name: MST Duet Reusable Handle for Single Use Heads Recalled by...

The Issue: Due to pin coming off of handles.

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

Class II — Potential Health HazardOngoing