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. 2,392 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,392 in last 12 months

Showing 1902119040 of 27,655 recalls

Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS 1-Piece IOL Recalled by Abbott Medical Optics Inc. (AMO) Due to...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS Symfony Extended Range of Vision IOL Recalled by Abbott Medical...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS Multifocal 1-Piece Intraocular Lens Recalled by Abbott Medical Optics...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Teleflex Medical

Recalled Item: Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised...

The Issue: The connector may disconnect from the tracheostomy tube during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS OptiBlue 1-Piece Intraocular Lens (IOL) Recalled by Abbott Medical...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS OptiBlue 1-Piece IOL with the TECNIS iTec Preloaded Delivery System...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2016· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Xhibit Telemetry Receiver (XTR) Recalled by Spacelabs...

The Issue: The firm received multiple reports of Xhibit Telemetry System going offline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2016· Sorin Group USA, Inc.

Recalled Item: St¿ckert S5 System Recalled by Sorin Group USA, Inc. Due to Sorin/LivaNova...

The Issue: Sorin/LivaNova is initiating a field correction on the S5 Heart-lung machine...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension IRON Flex reagent cartridges Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has become aware of deferoxamine interference...

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

Class III — Low RiskOngoing
Medical DeviceAugust 25, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista IRON Flex reagent cartridges Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has become aware of deferoxamine interference...

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

Class III — Low RiskOngoing
Medical DeviceAugust 25, 2016· CooperSurgical, Inc.

Recalled Item: Sage In-Vitro Fertilization- CSC (Choline Substituted Cryopreservation)...

The Issue: Products contain international package insert and not the correct USA...

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

Class III — Low RiskOngoing
Medical DeviceAugust 25, 2016· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...

The Issue: The firm received multiple reports of Xhibit Telemetry System going offline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2016· CooperSurgical, Inc.

Recalled Item: Sage In-Vitro Fertilization- CSC (Choline Substituted Cryopreservation)...

The Issue: Products contain international package insert and not the correct USA...

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

Class III — Low RiskOngoing
Medical DeviceAugust 24, 2016· Azer Scientific, Inc.

Recalled Item: Glucose Tolerance Beverage- Orange 50 gram Concentration Recalled by Azer...

The Issue: Out of Specification Microbiological test results

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Ingenuity Core 128 Model Number 728323 Product Usage: Computed Tomography...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Ingenuity Core Model Number 728321 Product Usage: Computed Tomography X-ray...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· ICU Medical, Inc.

Recalled Item: Tego Connector Recalled by ICU Medical, Inc. Due to ICU Medical Inc. has...

The Issue: ICU Medical Inc. has identified a potential risk of leaking with certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Philips Medical Systems

Recalled Item: Brilliance 64 CT Model Number 728231 Product Usage: Computed Tomography...

The Issue: The infant performance test did not meet the test specification for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Azer Scientific, Inc.

Recalled Item: Fruit Punch Glucose Recalled by Azer Scientific, Inc. Due to Out of...

The Issue: Out of Specification Microbiological test results

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2016· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Integra Cranial Access Kits Recalled by Integra LifeSciences Corp. d.b.a....

The Issue: Integra LifeSciences has been notified of a medical device recall by...

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

Class II — Potential Health HazardOngoing