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 4716147180 of 48,770 recalls

FoodAugust 24, 2012· MyoSci Technologies Inc.

Recalled Item: Whey Protein Concentrate Recalled by MyoSci Technologies Inc. Due to...

The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 24, 2012· MyoSci Technologies Inc.

Recalled Item: Whey Protein Isolate Cold-Filtration Recalled by MyoSci Technologies Inc....

The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 24, 2012· MyoSci Technologies Inc.

Recalled Item: Hydrolyzed Whey Protein High Grade Recalled by MyoSci Technologies Inc. Due...

The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 24, 2012· MyoSci Technologies Inc.

Recalled Item: Whey Protein Isolate MicroFiltration Recalled by MyoSci Technologies Inc....

The Issue: True Nutrition is recalling Whey Protein Isolate, Whey Protein Concentrate,...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 24, 2012· Iradimed Corporation

Recalled Item: The brand name is MRidium Series 1000 MR Infusion Sets Recalled by Iradimed...

The Issue: Iradimed Corporation is recalling MRidium Series 1000 MR Infusion Sets, Type...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: MX 16-slice CT Scanner System Recalled by Philips Medical Systems...

The Issue: On August 24, 2012 the firm recalled the MX 16-slice after discovering that...

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

Class II — Potential Health HazardOngoing
DrugAugust 23, 2012· Evol Nutrition

Recalled Item: Mojo Nights Recalled by Evol Nutrition Due to Marketed Without an Approved...

The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2012· Evol Nutrition

Recalled Item: Mojo Nights for Her Recalled by Evol Nutrition Due to Marketed Without an...

The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2012· Ferring Pharmaceuticals Inc

Recalled Item: Novarel¿ (Chorionic Gonadotropin for injection Recalled by Ferring...

The Issue: Labeling; incorrect or missing insert; Warnings portion of the Package...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 23, 2012· King Systems Corp.

Recalled Item: Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia...

The Issue: King Systems received a customer complaint indicating that the customer had...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 23, 2012· Biomet, Inc.

Recalled Item: Optilock 2.7 mm Screw Inserter. Intended Use: The OptiLock Upper Recalled by...

The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2012· Biomet, Inc.

Recalled Item: Optilock T15 AO Driver (3.5mm). Intended Use: The OptiLock Upper Recalled by...

The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2012· Viscot Medical LLC

Recalled Item: Dual Tip Marker Recalled by Viscot Medical LLC Due to Dual Tip Marker has...

The Issue: Dual Tip Marker has inconsistent ink flow on the black permanent ink side.

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

Class III — Low RiskOngoing
Medical DeviceAugust 22, 2012· SpineFrontier, Inc.

Recalled Item: S-Lift Implant Guides (also known as S-LIF) Compressor Part Number: Recalled...

The Issue: When using the optional S-LIFT (also known as S-LIF) Implant Guides without...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2012· DePuy Orthopaedics, Inc.

Recalled Item: S-Rom¿ Total Hip System Poly Liner Packaging: The insert is Recalled by...

The Issue: Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of four lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2012· Smith & Nephew Inc

Recalled Item: 12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW Recalled by Smith &...

The Issue: Modular necks were manufactured out of specification by a vendor; the taper...

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

Class II — Potential Health HazardOngoing
DrugAugust 21, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Adulterated...

The Issue: Adulterated Presence of Foreign Tablets: A product complaint was received by...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 21, 2012· Newark Nut Stores, Inc.

Recalled Item: Organic Pine Nuts (Raw Recalled by Newark Nut Stores, Inc. Due to Pine nuts...

The Issue: Pine nuts may contain peanuts

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 21, 2012· J F C International Inc

Recalled Item: Furikake (a Japanese rice seasoning of seaweed flakes with...

The Issue: The firm recalled the product due to undeclared eggs, soybeans, and wheat....

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 21, 2012· American Licorice Co

Recalled Item: Original Snaps Classic Chewy Candy Recalled by American Licorice Co Due to...

The Issue: CA Dept. of Public Health collected random samples of Red Vines Black...

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

Class II — Potential Health HazardOngoing
Refund