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. 2,450 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,450 in last 12 months

Showing 1880118820 of 48,770 recalls

Medical DeviceJanuary 28, 2020· Smith & Nephew, Inc.

Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...

The Issue: The spike rail was manufactured with an oversized thru-hole which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Smith & Nephew, Inc.

Recalled Item: JOURNEY II UNI RESECTION PREP TRIAL Recalled by Smith & Nephew, Inc. Due to...

The Issue: The spike rail was manufactured with an oversized thru-hole which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Medicrea International

Recalled Item: Pedicle Screws Recalled by Medicrea International Due to An internal...

The Issue: An internal component was assembled in the incorrect orientation, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Qiagen Sciences LLC

Recalled Item: QIAGEN Rotor Gene Q Software version 2.3.4. Real-time PCR analyzer Recalled...

The Issue: When using the Rotor-Gene Q with Software version 2.3.4 completing a LIMs...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Medicrea International

Recalled Item: Iliac Screws Recalled by Medicrea International Due to An internal component...

The Issue: An internal component was assembled in the incorrect orientation, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Medtronic, PLC

Recalled Item: McGRATH X3 Disposable Laryngoscope Blades-used with the McGRATH MAC Video...

The Issue: Blades do not fit the McGRATH MAC video laryngoscope handle or were tight...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2020· Breas Medical, Inc.

Recalled Item: Protective Cover Vivo 55/65 (Used for Vivo 50/65) Recalled by Breas Medical,...

The Issue: The outlet hole of the exhalation valve control pressure tube on the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 27, 2020· Teva Pharmaceuticals USA

Recalled Item: Methylphenidate hydrochloride Extended-Release ablets USP (CII) Recalled by...

The Issue: CGMP deviations: Product bottle may be absent of desiccant.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 27, 2020· Teva Pharmaceuticals USA

Recalled Item: Methylphenidate hydrochloride Extended-Release ablets USP (CII) Recalled by...

The Issue: CGMP deviations: Product bottle may be absent of desiccant.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 27, 2020· Teva Pharmaceuticals USA

Recalled Item: Desmopressin Acetate Tablets Recalled by Teva Pharmaceuticals USA Due to GMP...

The Issue: GMP Deviations: Product bottle may be absent of desiccant.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 27, 2020· Teva Pharmaceuticals USA

Recalled Item: Desmopressin Acetate Tablets Recalled by Teva Pharmaceuticals USA Due to GMP...

The Issue: GMP Deviations: Product bottle may be absent of desiccant.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 27, 2020· Exactech, Inc.

Recalled Item: Truliant Splined Stem Extension Recalled by Exactech, Inc. Due to These...

The Issue: These Truliant Splined Stem Extension, 18mm x 120mm were found to have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2020· Fridababy LLC

Recalled Item: fridababy SmileFrida the TOOTHHUGGER 18+ months Triple Angle Brush Cleans...

The Issue: FridaBaby has been made aware through customer reports that the product is...

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

Class II — Potential Health HazardOngoing
DrugJanuary 24, 2020· Breckenridge Pharmaceutical, Inc

Recalled Item: Solifenacin Succinate Tablets Recalled by Breckenridge Pharmaceutical, Inc...

The Issue: CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2020· Breckenridge Pharmaceutical, Inc

Recalled Item: Solifenacin Succinate Tablets Recalled by Breckenridge Pharmaceutical, Inc...

The Issue: CGMP Deviations: During manufacturing Solifenacin Succinate Tablets might...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2020· Ascend Laboratories LLC

Recalled Item: Olmesartan Medoxomil Tablets 20 mg Recalled by Ascend Laboratories LLC Due...

The Issue: cGMP Deviations; Olmesartan Medoximil Tablets 20 mg was released in error...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2020· Macleods Pharma Usa Inc

Recalled Item: Pioglitazone and Metformin Hydrochloride Tablets Recalled by Macleods Pharma...

The Issue: Subpotent Drug: Out of specification assay result, below specification, for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 24, 2020· bioMerieux, Inc.

Recalled Item: PREVI Isola Insrument and PREVI Isola Printer spares PSUs (power supply...

The Issue: The recall has been initiated due to potential for overheating or a fire...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2020· Abbott Gmbh & Co. KG

Recalled Item: LN 3R70-01 Recalled by Abbott Gmbh & Co. KG Due to Abbott has identified...

The Issue: Abbott has identified potential performance issues for the Alinity ci...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000...

The Issue: Potential exists for one or more axes of the robotic stand to become blocked...

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

Class II — Potential Health HazardOngoing