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. 2,355 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,355 in last 12 months

Showing 2658126600 of 27,655 recalls

Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 5.0 w/Needles with violet and blue Orthocord Product Number:...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 5.0mm with Panacryl without needles Product Number: 222965 SPIRALOK...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: SpiraLok 6.5 w/Needles with violet and blue Orthocord Product Number:...

The Issue: Fracture of SPIRALOK Anchors post op, requiring patient revision

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Hip Components: INSERT MOBILE "COLLEGIA" TAILLE 58*28 Recalled by Wright...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Extremity Components: PROTHESE A EXPANSION COMPLETE D=6 LG 12 MM Recalled by...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Wright Medical Technology Inc

Recalled Item: Knee Components: ROTULE "913" D=32 Recalled by Wright Medical Technology Inc...

The Issue: There may be inaccuracies on the labeled shelf life on all products packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Zimmer, Inc.

Recalled Item: ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended...

The Issue: Zimmer is conducting a voluntary removal of some Zimmer A.T.S. 3000...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray DPM5 Monitor Recalled by Mindray DS USA, Inc. d.b.a. Mindray North...

The Issue: Mindray has identified an issue with the DPM5 monitors where ST and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: NCB¿ screw ¿ 4.0 self-tapping Recalled by Zimmer, Inc. Due to Zimmer Inc.,...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: NCB¿-PT lateral proximal 3 hole tibial plate Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Sirus¿ intramedullary nail for tibia Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: MS-30¿ Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ Revision + set screw Recalled by Zimmer, Inc. Due to Zimmer Inc.,...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ Universal spacer 6-45 Recalled by Zimmer, Inc. Due to Zimmer Inc.,...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Inverse/Reverse Glenoid Sterile Recalled by Zimmer,...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Inverse Humeral Cup Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: zimmer Anatomical Shoulder Glenoid S Recalled by Zimmer, Inc. Due to Zimmer...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Biolox¿ Option Ceramic Femoral Head System Rx Recalled by Zimmer, Inc. Due...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Dynesys¿ Set screw M6 Recalled by Zimmer, Inc. Due to Zimmer Inc., is...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2012· Zimmer, Inc.

Recalled Item: Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile Recalled by...

The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...

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

Class II — Potential Health HazardOngoing