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. 2,272 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,272 in last 12 months

Showing 4592145940 of 48,770 recalls

Medical DeviceFebruary 26, 2013· Intio Inc

Recalled Item: INTIO Inc. Recalled by Intio Inc Due to INTIO Inc. distributed a SVM User's...

The Issue: INTIO Inc. distributed a SVM User's Manual and it has an editing mistake...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2013· Hill-Rom, Inc.

Recalled Item: TotalCare SpO2RT2 bed. Product Usage: Bed Recalled by Hill-Rom, Inc. Due to...

The Issue: In certain situations a software problem with the TotalCare SpO2RT¿ 2 bed...

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

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2013· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Visible particulate embedded in vials was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set (6") with Twist Clamp. Recalled by...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set. Product Code 5C4449. intended...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: CAPD Solution Transfer Set with Locking Connector. Product Code: 5C4160....

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set Extra Short (4") with Recalled by...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog # 42214...

The Issue: Glucose test strips reports no result message when tested

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog #...

The Issue: Glucose test strips reports no result message when tested

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Lifescan Inc

Recalled Item: LifeScan brand OneTouch¿ Select Control Solution Recalled by Lifescan Inc...

The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Nipro Diagnostics, Inc.

Recalled Item: Duane Reade TRUEtrack monitor kit Recalled by Nipro Diagnostics, Inc. Due to...

The Issue: Meter kit outer boxes containing 10 ct. test strips state incorrect storage...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Lifescan Inc

Recalled Item: LifeScan brand OneTouch¿ Ultra Control Solution Recalled by Lifescan Inc Due...

The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· DePuy Orthopaedics, Inc.

Recalled Item: ReClaim Reamer Extension Recalled by DePuy Orthopaedics, Inc. Due to The...

The Issue: The tabs on the reamer extension device have broken. DePuy is notifying...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Symbios Medical Products, LLC

Recalled Item: GOPump Elastometric infusion PumpKit with/ and without accesssories all...

The Issue: Received 2 complaints out of 458 distributed pumps in this lot, where flow...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 24, 2013· Clinical Diagnostic Solutions

Recalled Item: Boule Con-Diff Tri-Level Multi-Parameter Assayed Hematology Control Recalled...

The Issue: Elevated MCV results on the 1311-682, 1311-683, and 1311-684 lots.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Baseplate Impactor Extractor TRIATHLON Instruments....

The Issue: Stryker received reports from the field indicating that the handle detached...

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

Class II — Potential Health HazardOngoing
DrugFebruary 22, 2013· Lupin Pharmaceuticals Inc.

Recalled Item: Ethambutol Hydrochloride Tablets USP Recalled by Lupin Pharmaceuticals Inc....

The Issue: Failed Impurities/Degradation Specifications: This product is being recalled...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 22, 2013· Lion Pavilion Ltd.

Recalled Item: Grassplot Ginger Slice Recalled by Lion Pavilion Ltd. Due to Undeclared Sulfites

The Issue: The product contained undeclared sulfites (735 ppm) based on sampling and...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 22, 2013· The King Arthur Flour Company, Inc.

Recalled Item: King Arthur Unbleached Bread Flour Recalled by The King Arthur Flour...

The Issue: Foreign material

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 22, 2013· The King Arthur Flour Company, Inc.

Recalled Item: King Arthur Unbleached All-Purpose Flour Recalled by The King Arthur Flour...

The Issue: Foreign material

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

Class II — Potential Health HazardOngoing
Refund