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. 2,279 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,279 in last 12 months

Showing 4408144100 of 48,770 recalls

DrugJuly 25, 2013· Hi-Tech Pharmacal Co., Inc.

Recalled Item: Clobetasol Propionate Cream Recalled by Hi-Tech Pharmacal Co., Inc. Due to...

The Issue: Labeling: Label Mix-up; some cartons labeled as Clobetasol Propionate Cream...

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

Class III — Low RiskOngoing
Refund
FoodJuly 25, 2013· Thrive Foods LLC

Recalled Item: THRIVE 6 Grain Pancake Mix Recalled by Thrive Foods LLC Due to Thrive Foods...

The Issue: Thrive Foods is recalling certain lots of its 64 and 72 ounce cans of THRIVE...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 25, 2013· Velocity Medical Solutions, LLC

Recalled Item: DICOM Export Format for Sum Dose with Velocity v3.0.0. A Recalled by...

The Issue: An anomaly was detected such that, under certain conditions, a summed dose...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Medtronic Navigation, Inc.

Recalled Item: Medtronic O-arm Imaging System Mobile X-ray system. Model No. BI-700-00027...

The Issue: Review of on-system electronic product labeling and Instructions for comply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· HemoCue AB

Recalled Item: HemoCue¿ Hb 201 Microcuvettes Recalled by HemoCue AB Due to HemoCue AB has...

The Issue: HemoCue AB has become aware of a production related problem involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Advanced Sterilization Products

Recalled Item: STERRAD 100NX Cassettes Recalled by Advanced Sterilization Products Due to...

The Issue: The recall of the STERRAD 100NX Cassettes was initiated because Advanced...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Folate (2500 tests) Recalled by Siemens Healthcare...

The Issue: Calibration failures and/or significant negative shifts in quality control...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Folate (500 Tests) SMN 10325366 Recalled by Siemens Healthcare...

The Issue: Calibration failures and/or significant negative shifts in quality control...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Roche Molecular Systems, Inc.

Recalled Item: KIT cobas 4800 HPV AMP/DET 240T / 960T US-IVD Recalled by Roche Molecular...

The Issue: During an internal investigation, a formulation error that occurred was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Folate (500 tests) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Calibration failures and/or significant negative shifts in quality control...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Folate (100 Tests) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Calibration failures and/or significant negative shifts in quality control...

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

Class II — Potential Health HazardOngoing
DrugJuly 24, 2013· Baxter Healthcare Corp.

Recalled Item: DIANEAL Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 1.5%...

The Issue: Defective Container: There is a potential for frangible components to be...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 24, 2013· Gyrus Medical, Inc

Recalled Item: GYRUS ACMI Recalled by Gyrus Medical, Inc Due to On April 29, 2013 Olympus...

The Issue: On April 29, 2013 Olympus Surgical Technologies America R&D received results...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2013· OrthoPediatrics Corp

Recalled Item: 3.2mm Drill Bit. This is a component within the PediLoc Recalled by...

The Issue: OrthoPediatrics has initiated a voluntary recall of Part # 01-1050-002,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2013· Nestle HealthCare Nutrition

Recalled Item: Nestle Nutrition Recalled by Nestle HealthCare Nutrition Due to Nestle...

The Issue: Nestle HealthCare Nutrition, Inc. is initiating a recall on some of Compat...

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

Class II — Potential Health HazardOngoing
DrugJuly 23, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Terazosin Hydrochloride Capsules Recalled by Teva Pharmaceuticals USA, Inc....

The Issue: Labeling -label error on declared strength: unopened, sealed bottle of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2013· Elekta, Inc.

Recalled Item: Stereotactic Circular Collimator - 3D Line stereotatic Hardware Accessories...

The Issue: Potential for clinical errors.

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

Class II — Potential Health HazardOngoing
DrugJuly 22, 2013· Mira Health Products Ltd.

Recalled Item: Super-DMZ Rx 2.0 Capsules Recalled by Mira Health Products Ltd. Due to...

The Issue: Marketed without an Approved NDA/ANDA; product contains the steroid...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 22, 2013· Mira Health Products Ltd.

Recalled Item: B-50 capsules Recalled by Mira Health Products Ltd. Due to Marketed without...

The Issue: Marketed without an Approved NDA/ANDA; product found to contain methasterone...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 22, 2013· Mira Health Products Ltd.

Recalled Item: METHA-DROL Extreme capsules Recalled by Mira Health Products Ltd. Due to...

The Issue: Marketed without an Approved NDA/ANDA; product found to contain dimethazine...

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

Class I — Serious Health HazardOngoing
Refund