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. 2,366 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,366 in last 12 months

Showing 2382123840 of 27,655 recalls

Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2014· Gen-Probe Inc

Recalled Item: APTIMA Urine Collection Kit Recalled by Gen-Probe Inc Due to Incorrect...

The Issue: Incorrect labeling was used on each pouch of the affected lots of APTIMA...

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

Class III — Low RiskOngoing
Medical DeviceApril 17, 2014· Mckesson Medical Immaging

Recalled Item: McKesson Radiology-PACS. McKesson Radiology is a medical image and...

The Issue: High priority alert icon was not displayed in the Study List when there are...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Test Strips Recalled by Alere San Diego,...

The Issue: Test Strips may report an inaccurately low INR result. Several patients had...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 16, 2014· Synthes, Inc.

Recalled Item: DePuy Synthes Craniomaxillofacial Distraction System (AB Distractor Bodies...

The Issue: DePuy Synthes is initiating a recall of certain lots of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 16, 2014· Sakura Finetek USA Inc

Recalled Item: Tissue-Tek PARAFORM PROC/EMB/MEDIUM Recalled by Sakura Finetek USA Inc Due...

The Issue: This Lot has variations in melting temperature.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Maquet Medical Systems USA

Recalled Item: Maquet PowerLED 700. Product Usage Recalled by Maquet Medical Systems USA...

The Issue: Maquet has identified an issue with the Maquet PowerLED 700 (certain serial...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Passer Recalled by Biomet, Inc. Due to The nitinol wire or...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Suture Retriever Recalled by Biomet, Inc. Due to The nitinol wire or...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Brainlab AG

Recalled Item: ExacTrac 5.5 Recalled by Brainlab AG Due to When using a specific plan...

The Issue: When using a specific plan update workflow in combination with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Fisher & Paykel Healthcare, Ltd.

Recalled Item: Infant Nasal CPAP (continuous positive airway pressure) Prong Recalled by...

The Issue: The Infant Nasal CPAP Prong has the potential to detach from the Nasal...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 15, 2014· Biomet, Inc.

Recalled Item: EZPass Nylon Monofilament Single Pack Recalled by Biomet, Inc. Due to The...

The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2014· Handicare USA, Inc.

Recalled Item: ReTurn 7500/7500 Aid Recalled by Handicare USA, Inc. Due to During the...

The Issue: During the period of April 2009  May 2011, Handicare AB used a wing handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Laureate Hydrophilic Guide Wire Recalled by Merit Medical Systems,...

The Issue: Discrepancy between the carton and unit labeling for the Merit Laureate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Laureate 0.035" (0.89mm) Hydrophilic Guide Wire Recalled by Merit...

The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Disposable Centrifugal Pump with X-Coating Recalled by Terumo...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Ivoclar Vivadent, Inc.

Recalled Item: bluephase style Light probe Pin-point 6>2 mm black REF # Recalled by Ivoclar...

The Issue: A stock check revealed broken glass fibers between the connector and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus...

The Issue: Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips...

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

Class II — Potential Health HazardOngoing