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 2556125580 of 27,655 recalls

Medical DeviceApril 30, 2013· Angiodynamics, Inc.

Recalled Item: AngioDynamics VenaCure EVLT NeverTouch-FRS PROCEDURE KIT under the following...

The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· TZ Medical Inc.

Recalled Item: adult defibrillation Recalled by TZ Medical Inc. Due to TZ Medical Inc is...

The Issue: TZ Medical Inc is recalling its P-211-M1 and P-214-M1 Medtronic / Physio...

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: AsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one...

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· Hill-Rom, Inc.

Recalled Item: SlingBar 350. Designed to meet the needs for lifting humans. Recalled by...

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 360. Designed to meet the needs for lifting humans. Recalled by...

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· American Optisurgical Inc

Recalled Item: FAST Procedure Kit. Intended for use as a Minor Surgical Procedures Tray....

The Issue: American Optisurgical, Inc initiated a recall of ChloraPrep Hi-Lite Orange...

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 Medication Cup. For the delivery of liquid medications Recalled...

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· American Optisurgical Inc

Recalled Item: TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1...

The Issue: American Optisurgical, Inc. is recalling certain lots of TX1 Tissue Removal...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2013· Angiodynamics, Inc.

Recalled Item: AngioDynamics Micro Introducer Kits under the following labeling: 1)...

The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2013· Biomet, Inc.

Recalled Item: Biomet Trauma Phoenix Retrograde Femoral Connecting Bolt Trauma Fixation...

The Issue: Biomet Trauma ("Biomet") has initiated a recall of Retrograde Femoral...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Cardio Medical Products

Recalled Item: Cardio Medical Products Recalled by Cardio Medical Products Due to Covidien...

The Issue: Covidien received customer reports of Arcing/Sparking on the defibrillation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2013· Beckman Coulter Inc.

Recalled Item: AU2700 Clinical Chemistry Analyzer AU5400 Clinical Chemistry Analyzer...

The Issue: Beckman Coulter is recalling AU2700/AU2700 Plus & AU5400 Clinical Chemistry...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is...

The Issue: Siemens has confirmed that the TACR method may demonstrate reduced on-board...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView SPECT gamma camera for Emission Computed Tomography Recalled by...

The Issue: Philips has received one report from the field that there was an unexpected...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Hologic, Inc.

Recalled Item: Fluoroscan Mini C-arm InSight Recalled by Hologic, Inc. Due to The audible...

The Issue: The audible alarm to alert the operator when cumulative irradiation time...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: B-CrossLaps/serum (B-CTx in serum) 160 100 tests Immunoassay Recalled by...

The Issue: Roche Diagnostics internal investigations in R&D have shown that the claims...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Leibel-Flarsheim Company LLC

Recalled Item: Hydra Vision DR 60/80 System Recalled by Leibel-Flarsheim Company LLC Due to...

The Issue: A complaint was received in which a hospital physicist indicated the dosage...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· Instratek, Incorporated

Recalled Item: Mini Cannulated Titanium Headed and Headless Screw Set and 2.5 Recalled by...

The Issue: Faded and wrong markings on bone screw Countersink/Depth Gauge instruments...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******microMax Handpiece***Rx Only***Manufacturer: The Anspach Effort...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2013· The Anspach Effort, Inc.

Recalled Item: ******Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort Recalled by...

The Issue: The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary...

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

Class II — Potential Health HazardOngoing