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. 2,661 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,661 in last 12 months

Showing 2246122480 of 29,505 recalls

Medical DeviceOctober 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...

The Issue: The following MRx software issue has been identified: MRx model M3535A with...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm)...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Stryker Sustainability Solutions

Recalled Item: SSS Reprocessed Zimmer Recalled by Stryker Sustainability Solutions Due to...

The Issue: It was reported that packaging was not properly sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2015· Stryker Medical Division of Stryker Corporation

Recalled Item: Two-stage and three-stage I.V. poles are shipped as an optional Recalled by...

The Issue: It was identified by a customer complaint that some I.V. poles were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2015· Ceterix Orthopedics, Inc.

Recalled Item: NovoCut Suture Manager Recalled by Ceterix Orthopedics, Inc. Due to The...

The Issue: The NovoCut Suture Manager device may cut the suture during knot tensioning...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2015· Beckman Coulter Inc.

Recalled Item: Access CEA Assay Recalled by Beckman Coulter Inc. Due to Beckman Coulter is...

The Issue: Beckman Coulter is recalling the Access CEA reagent packs because they were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2015· Event Medical LTD

Recalled Item: Inspiration Ventilator System Recalled by Event Medical LTD Due to A...

The Issue: A component on the systems power board can fail in a manner which can cause...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 9, 2015· CareFusion 303, Inc.

Recalled Item: SmartSite Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...

The Issue: CareFusion is recalling the SmartSite Extension Set due to disconnection and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2015· Miramar Labs, Inc.

Recalled Item: miraDry System consisting of the MD4000-MC Console Recalled by Miramar Labs,...

The Issue: Update to labeling for the miraDry Console to remind users to only use...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2015· Boston Scientific Corporation

Recalled Item: RotaWire Elite and wireClip Torquer Recalled by Boston Scientific...

The Issue: Boston Scientific is recalling its recently released RotaWire Elite...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 9, 2015· Boston Scientific Corporation

Recalled Item: RotaWire Elite and wireClip Torquer Recalled by Boston Scientific...

The Issue: Boston Scientific is recalling its recently released RotaWire Elite...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 8, 2015· Precision Medical, Inc.

Recalled Item: Easy Dial Oxygen Regulator Recalled by Precision Medical, Inc. Due to These...

The Issue: These lots of Oxygen Dial Regulators could have the settings label off by...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2015· Ivoclar A. G.

Recalled Item: Helioseal F Sealant 1 x 1.25 g Recalled by Ivoclar A. G. Due to A defect...

The Issue: A defect occurred in the production process of Helioseal F Sealant; the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2015· Hill-Rom, Inc.

Recalled Item: Hill-Rom 100 Low Bed (GPAC) AC Powered adjustable hospital bed Recalled by...

The Issue: Hill-Rom is voluntarily recalling the Hill-Rom 100 Low Bed due to complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes Threaded Plate Holder- Long for 3.5mm Locking Hold Recalled by...

The Issue: The affected part number and lot listed above is incorrectly etched with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2015· Cyberonics, Inc

Recalled Item: Cyberonics Vagus Nerve Stimulator (VNS) Therapy AspireSR Generator Recalled...

The Issue: Certain Model 106 Pulse Generators demonstrate delays in sensing during use...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry XPT Systems Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Multiple Software issues. Auto Start-UP Fail, Calibration Interval Resets...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2015· Cook Inc.

Recalled Item: Shuttle Select Slip-Cath Catheter. Angiographic catheter. For use in...

The Issue: Reports of catheter tip splits and or separation. Loss of device function,...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 2, 2015· C.R. Bard, Inc.

Recalled Item: Antibacterial Hydro Personal Catheter Recalled by C.R. Bard, Inc. Due to...

The Issue: Incorrect unit labeling. The case label and shelf box are correct, Product...

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

Class III — Low RiskOngoing
Medical DeviceOctober 2, 2015· Welch Allyn Inc

Recalled Item: Welch Allyn KleenSpec Corded Illumination System Recalled by Welch Allyn Inc...

The Issue: The firm became aware that the KleenSpec¿ 788 Corded Illuminator has the...

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

Class II — Potential Health HazardOngoing