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. 989 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
989 in last 12 months

Showing 29881–29900 of 48,770 recalls

Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 14mmdx50cm right Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 16mmdx46cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 16mmdx42cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Por fullct fem st 15x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 15mmdx48cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Stryker Communications

Recalled Item: The Stryker Visum¿ LED Surgical Lighting system is intended to Recalled by...

The Issue: The potential hazard that can arise for the combination of the missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 15mmdx46cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Zee and Zeego fluoroscopic x-ray system Recalled by Siemens Medical...

The Issue: A gap in the housing of the wireless foot switch could potentially result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q and Q.Zen fluoroscopic x-ray system Recalled by Siemens Medical...

The Issue: A gap in the housing of the wireless foot switch could potentially result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Welch Allyn Inc

Recalled Item: Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400 Recalled by Welch...

The Issue: A defective electrical component in the battery charging circuit in two lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Zimmer Biomet, Inc.

Recalled Item: MEDTECH ROSA Brain 3.0 The device is intended for the Recalled by Zimmer...

The Issue: Unapproved change made by the supplier.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Axiom Artis fluoroscopic x-ray system Recalled by Siemens Medical Solutions...

The Issue: A gap in the housing of the wireless foot switch could potentially result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2017· Zimmer Biomet, Inc.

Recalled Item: MEDTECH ROSA Spine 1.0.2 The device is intended for the Recalled by Zimmer...

The Issue: Unapproved change made by the supplier.

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

Class II — Potential Health HazardOngoing
FoodFebruary 27, 2017· Versa Marketing

Recalled Item: Fusia Asian Aspirations Szechuan Stir Fry Recalled by Versa Marketing Due to...

The Issue: Product was tested and found positive for Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2017· Manzana Products Co., Inc.

Recalled Item: Trader Joe's First Crush Unsweetened Gravenstein Apple Sauce Recalled by...

The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2017· Manzana Products Co., Inc.

Recalled Item: Trader Joe's Organic Unsweetened Apple Sauce Recalled by Manzana Products...

The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2017· Manzana Products Co., Inc.

Recalled Item: Trader Joe's All Natural Unsweetened Apple Sauce Recalled by Manzana...

The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 24, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X 3/8 model number 882478 BrightView and BrightView X Recalled by...

The Issue: The brake hub was not engaging with the gear box shaft due to an error in...

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

Class III — Low RiskOngoing