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 2554125560 of 27,655 recalls

Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - Calf Garment Standard Ref. L501-M Lot 122549 Recalled by Surgical...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: -Instratek Carpal Tunnel Release Blades Recalled by Surgical Instrument...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: -Scorpion Needle Recalled by Surgical Instrument Service And Savings, Inc....

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - CLEAR-TRAC COMPLETE Recalled by Surgical Instrument Service And Savings,...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: - Relieva Flex Sinus Guide Catheter (Green) Tip Shape: F-70 Recalled by...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2013· Surgical Instrument Service And Savings, Inc.

Recalled Item: Large Tear Cross Cut Rasp 14mm x 7mm Ref. 5100-37-114 Recalled by Surgical...

The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens brand MicroScan Dried Negative Breakpoint Combo 47 panels...

The Issue: The product has the potential for false negative or delayed reaction for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Merit Medical Systems, Inc.

Recalled Item: Merit Medical PerfOrma Anglographic Catheter 5F Multipack Product Usage:...

The Issue: Merit Medical Systems is recalling various lots of Performa Cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Remel Inc

Recalled Item: Streptex* Latex D Recalled by Remel Inc Due to The product may give weak or...

The Issue: The product may give weak or false negative test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2013· Remel Inc

Recalled Item: Streptex* kit Recalled by Remel Inc Due to The product may give weak or...

The Issue: The product may give weak or false negative test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Becton Dickinson & Company

Recalled Item: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes...

The Issue: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Becton Dickinson & Company

Recalled Item: BD SafetyGlide Allergy. Sterile Allergy Treatment Syringe Tray. Recalled by...

The Issue: There has been an increase in complaints regarding the needle/safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Applied Medical Resources Corp

Recalled Item: Applied Medicals Epix¿ and Direct Drive Laparoscopic Graspers Recalled by...

The Issue: Applied Medical is conducting a voluntary recall on specific lot numbers of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· Elekta, Inc.

Recalled Item: DMLC IV-ERGO Product Usage: Intended for use with rotating gantry Recalled...

The Issue: It is possible for an intermittent error to occur in the gantry sensor of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2013· CooperSurgical, Inc.

Recalled Item: CooperSurgical TransWarmer Infant Transport Mattress with WarmGel P/N 20421...

The Issue: Trans Warmer Infant and Transport Mattress not labeled with exp.date may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Nephron Pharmaceuticals Corp.

Recalled Item: EZ Breathe Atomizer Model # EZ-100. For the delivery of Recalled by Nephron...

The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 30, 2013· Elekta, Inc.

Recalled Item: Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated...

The Issue: Unexpected movement during beam delivery may not be detected if there are...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Hill-Rom, Inc.

Recalled Item: SlingBar Standard. Designed to meet the needs for lifting humans. Recalled...

The Issue: Retrospective review found 4 sling bars that may present a potential for...

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

Class II — Potential Health HazardOngoing