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. 2,266 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,266 in last 12 months

Showing 4662146640 of 48,770 recalls

Medical DeviceOctober 26, 2012· Hospira Inc.

Recalled Item: Plum A+ Single Channel Infusion Pumps with Hospira Mednet Software Recalled...

The Issue: The volume control knob on some Plum A+ single channel infusers (located on...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2012· iwalk inc

Recalled Item: BiOM Rechargeable Li Ion 22.2 V Battery and BiOM Lithium Recalled by iwalk...

The Issue: Battery may over-heat during charging and smoke

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

Class II — Potential Health HazardOngoing
DrugOctober 25, 2012· Hospira Inc.

Recalled Item: Epinephrine Injection USP Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulates; may contain glass particles

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 25, 2012· Red Chamber Company

Recalled Item: Frozen Yellowfin Tuna Loin 3/5 Recalled by Red Chamber Company Due to Red...

The Issue: Red Chamber is recalling Frozen Yellowfin Tuna Loin due to customer...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 25, 2012· Philips Healthcare Inc.

Recalled Item: Philips DigitalDiagnost X-Ray System with Eleva Software 2.1.3 Model numbers...

The Issue: When the operator for a wall stand view selects an "image rotation"...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Hoffman LRF Wire Bolt Recalled by Stryker Howmedica Osteonics Corp. Due to...

The Issue: Two complaints have been filed where Hoffman LRF Wires have broken during...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Carl Zeiss Meditec, Inc.

Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...

The Issue: A manufacturing defect has been identified which could results in the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Quasar Bio-Tech, Inc. dba Silver Bay LLC

Recalled Item: Quasar Power Pack contains a Baby Quasar and a Baby Recalled by Quasar...

The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Quasar Bio-Tech, Inc. dba Silver Bay LLC

Recalled Item: Baby Quasar (LAB-001-D Recalled by Quasar Bio-Tech, Inc. dba Silver Bay LLC...

The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Quasar Bio-Tech, Inc. dba Silver Bay LLC

Recalled Item: Quasar MD is an infrared LED lamp that is labeled Recalled by Quasar...

The Issue: Quasar Bio-Tech is recalling their Baby Quasar, Baby Quasar Pink, Quasar...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Verathon, Inc.

Recalled Item: The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that...

The Issue: Re-usable video laryngoscope blades of the GlideScope GVL3, GVL4, and GVL5...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 25, 2012· Carl Zeiss Meditec, Inc.

Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...

The Issue: A manufacturing defect has been identified which could results in the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Carl Zeiss Meditec, Inc.

Recalled Item: INTRABEAM Balloon Applicator Set Recalled by Carl Zeiss Meditec, Inc. Due to...

The Issue: A manufacturing defect has been identified which could results in the small...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2012· Kerr Corporation

Recalled Item: BioPlant Recalled by Kerr Corporation Due to The firm initiated the recall...

The Issue: The firm initiated the recall becaue disturbing the BioPlant product soon...

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

Class II — Potential Health HazardOngoing
DrugOctober 24, 2012· GlaxoSmithKline, LLC.

Recalled Item: Advair HFA (fluticasone propionate 45 mcg and salmeterol 21 mcg) Recalled by...

The Issue: Product Lacks Stability: These lots are being recalled due to the failure to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 24, 2012· GlaxoSmithKline, LLC.

Recalled Item: Advair HFA (fluticasone propionate/salmeterol) Inhalation Aerosol Recalled...

The Issue: Product Lacks Stability: These lots are being recalled due to the failure to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodOctober 24, 2012· BumbleBar, Inc.

Recalled Item: Gluten Free Cafe Chocolate Sesame Bar. The Retail Carton has Recalled by...

The Issue: Gluten Free Cafe Chocolate Sesame Bar is recalled due to the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 24, 2012· BumbleBar, Inc.

Recalled Item: Gluten Free Cafe Cinnamon Sesame Bar. The Retail Carton has Recalled by...

The Issue: Gluten Free Cafe Cinnamon Sesame Bar is recalled due to the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 24, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: B. Braun Medical Inc. has become aware of an issue with the Outlook ES...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Sekisui Diagnostics Llc

Recalled Item: Sekisui Diagnostics Recalled by Sekisui Diagnostics Llc Due to Spectrolyse...

The Issue: Spectrolyse PAI-1 activity assay, producing lower than expected absorbance...

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

Class II — Potential Health HazardOngoing