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. 2,831 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,831 in last 12 months

Showing 57815800 of 29,505 recalls

Medical DeviceAugust 10, 2023· Turncare, Inc

Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...

The Issue: A software update corrected an issue where "low" and "terminal" battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Covidien

Recalled Item: McGrath Mac 2 Recalled by Covidien Due to Laryngoscope blades may contain an...

The Issue: Laryngoscope blades may contain an ineffective application of anti-fog agent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Covidien

Recalled Item: McGrath Mac 2 Recalled by Covidien Due to Laryngoscope blades may contain an...

The Issue: Laryngoscope blades may contain an ineffective application of anti-fog agent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Endobronchial Always on Track Models: INS-0392 AOTT 21ga Needle...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Percutaneous Always on Track Models: INS-5040 Always-On vTrack...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran:SPiN Thoracic Navigation System Models: SYS-4230 SPiN Thoracic...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Percutaneous Models: INS-5620 SPiN Perc Biopsy Needle Guide Kit -...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran : Endobronchial Models: INS-5500 View Optical Probe INS-5450 SPiN...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Olympus Corporation of the Americas

Recalled Item: Veran Endobronchial: Models: INS-5925 SPiN Access Catheter¿ 180 Degree for...

The Issue: Non-conformances in Veran devices (ig4 Image Guided System, SPiN Thoracic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Bard Peripheral Vascular Inc

Recalled Item: Bard Marquee Disposable Core Biopsy Instrument Kit Recalled by Bard...

The Issue: Diameter mismatch between coaxial and biopsy needle (cutting cannula) in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Epiphany Cardio Server E3 ECG Management System Servers with Recalled...

The Issue: Epiphany, now a Baxter Healthcare company, is issuing an Urgent Medical...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· ARROW INTERNATIONAL Inc.

Recalled Item: Arrow ErgoPack Pressure Injectable One-Lumen PICC Recalled by ARROW...

The Issue: This recall has been initiated due to reports that the product code and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· ARROW INTERNATIONAL Inc.

Recalled Item: Arrow ErgoPack Recalled by ARROW INTERNATIONAL Inc. Due to This recall has...

The Issue: This recall has been initiated due to reports that the product code and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· ETHICON, LLC

Recalled Item: PDS Plus Antibacterial (polydioxanone) Suture Recalled by ETHICON, LLC Due...

The Issue: Internal testing on returned product from this lot confirmed that some PDS"...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· ETHICON, LLC

Recalled Item: PDS II (polydioxanone) Suture Recalled by ETHICON, LLC Due to Internal...

The Issue: Internal testing on returned product from this lot confirmed that some PDS"...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Baxter Healthcare Corporation

Recalled Item: Welch Allyn Connex Spot Monitor Recalled by Baxter Healthcare Corporation...

The Issue: Product is being recalled due to the improper placement of a copper tape on...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Proboscis/Piston Assembly Recalled by Ortho-Clinical Diagnostics, Inc. Due...

The Issue: Ortho Clinical Diagnostics (QuidelOrtho) confirmed certain Proboscis/Piston...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2023· O&M HALYARD, INC.

Recalled Item: FLUIDSHIELD 3 N95 Particulate Filter Respirator and Surgical Mask with...

The Issue: One respirator sample failed a filtration efficiency test. This respirator...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· FX SHOULDER

Recalled Item: Centered Glenosphere w/Screw Recalled by FX SHOULDER Due to Centered...

The Issue: Centered glenosphere box may contain an eccentric glenosphere.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 3ML Syringe Luer Lock with needle 20GX1 Recalled by Fresenius Medical Care...

The Issue: There is a potential for blood backfill leakage and foreign material.

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

Class I — Serious Health HazardOngoing