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. 2,317 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,317 in last 12 months

Showing 4194141960 of 48,770 recalls

FoodFebruary 28, 2014· Mars Food US

Recalled Item: UNCLE BEN's(R) READY RICE(R) Original Enriched Long Grain White Rice...

The Issue: Voluntary recall was initiated after identifying a number of packages with...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 28, 2014· High Mowing Organic Seed

Recalled Item: High Mowing Organic Sprouting Seeds Ancient Eastern Blend Recalled by High...

The Issue: Contains undeclared wheat

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 28, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer Recalled by Roche...

The Issue: electrode used beyond the guaranteed in-use 52 week lifetime,may leak and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· Teleflex Medical

Recalled Item: Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube...

The Issue: The product may fail to achieve seal of right lung due to the cuff inflating...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound...

The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· Philips Medical Systems North America Inc.

Recalled Item: Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound...

The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. K102239...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Medtronic Neuromodulation

Recalled Item: Medtronic Activa RC (37612) Recalled by Medtronic Neuromodulation Due to...

The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Medtronic Neuromodulation

Recalled Item: Medtronic neurostimulators. Restore (37711) Recalled by Medtronic...

The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Medtronic Neuromodulation

Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic...

The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Bio-Rad Laboratories, Inc.

Recalled Item: D-10" Hemoglobin Testing System Recalled by Bio-Rad Laboratories, Inc. Due...

The Issue: On a rare occasion the D-10 software might generate an extra result by...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2014· Bard Access Systems

Recalled Item: PowerPort Slim Implantable Port Recalled by Bard Access Systems Due to...

The Issue: Labeling discrepancy.The label states that the implantable port contains...

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

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2014· Pfizer Us Pharmaceutical Group

Recalled Item: Advil PM Caplets Recalled by Pfizer Us Pharmaceutical Group Due to Subpotent...

The Issue: Subpotent Drug: This lot is being recalled because of out-of-specification...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 26, 2014· HP Hood LLC

Recalled Item: my essentials brand sour cream Recalled by HP Hood LLC Due to Foreign Object...

The Issue: HP Hood LLC received one complaint of a foreign object in sour cream product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 26, 2014· Leica Microsystems, Inc.

Recalled Item: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...

The Issue: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2014· Biomet, Inc.

Recalled Item: Part 475630 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...

The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2014· Biomet, Inc.

Recalled Item: Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm Recalled by...

The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw.The Saw...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2014· Biomet, Inc.

Recalled Item: Part 475625 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...

The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Hospira Inc.

Recalled Item: LifeShield LATEX-FREE HemoSet 100 mL Burette I.V. PlumSet Recalled by...

The Issue: Hospira identified an incorrect lower lid (set component) had been supplied...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2014· Zimmer, Inc.

Recalled Item: Natural-Knee¿/Apollo" Knee: M/B PAT SZ0 NATURAL-KNEE M/B PAT SZ1...

The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...

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

Class II — Potential Health HazardOngoing