Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,392 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,392 in last 12 months

Showing 2048120500 of 27,655 recalls

Medical DeviceDecember 22, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo Plaza Picture archiving and communication system. Software only. PACS...

The Issue: Siemens is releasing an updated software version to address several software...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Draeger Medical, Inc.

Recalled Item: Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus...

The Issue: Drager became aware of situations where the error message "Poti unplugged"...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: STD KIT GK260 Recalled by Applied Medical Resources Corp Due to Applied...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Cook Medical Incorporated

Recalled Item: Zilver¿ 518RX Vascular Stent with Rapid Exchange Delivery System Recalled by...

The Issue: Manufacturing of the joint between the inner catheter and stylet of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: STD KIT GK213 Recalled by Applied Medical Resources Corp Due to Applied...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: STD GK258 Recalled by Applied Medical Resources Corp Due to Applied Medical...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: CA500 Epix Universal Clip Applier Product Usage: The Epix disposable...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Ultradent Products, Inc.

Recalled Item: InterGuard 5.5mm Econo Recalled by Ultradent Products, Inc. Due to Ultradent...

The Issue: Ultradent is recalling InterGuard 5.5mm Econo , lot#s BC2GN and BC4L7...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Northeast Laboratory Services, Inc.

Recalled Item: NEL- GBS Medium (Broth 3 ml Fill 13 x 100 mm Screw Cap Tube Catalog No.:...

The Issue: Product marketed without a 510 (k)

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Northeast Laboratory Services, Inc.

Recalled Item: NEL GBS Medium 20 ml in 100x15mm plate (Standard Petri Dish) Catalog No.:...

The Issue: Product marketed without a 510 (k)

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Increased U90-382 or...

The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· ConMed Corporation

Recalled Item: Hip Preservation System Signature Series PreBent Burs under the following...

The Issue: Metal shavings released from burs during use are due to contact between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Baxter Corporation Englewood

Recalled Item: Baxter Recalled by Baxter Corporation Englewood Due to All lots of RAPIDFILL...

The Issue: All lots of RAPIDFILL Syringe Strips lack evidence supporting the packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Therakos Inc

Recalled Item: The THERAKOS CELLEX Photopheresis System is a photoimmune therapy. Catalog...

The Issue: The Mallinckrodt (Therakos) post-market monitoring process detected an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 350 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 250 Chemistry Systems Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2015· Stryker Spine

Recalled Item: Stryker Aero-AL Impaction handle Catalog Number 48921007. Stryker Spine...

The Issue: Reported jamming of the impaction handle when assembled to the Inserter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2015· NeoCoil, LLC

Recalled Item: NeoCoil 3.0T GEM Flex Coil. The 3.0T GEM Flex coil Recalled by NeoCoil, LLC...

The Issue: Potential for higher than specified surface temperatures. Use of 3.0T GEM...

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

Class II — Potential Health HazardOngoing