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 1882118840 of 48,770 recalls

DrugJanuary 22, 2020· Ascend Laboratories LLC

Recalled Item: Minocycline Hydrochloride Extended-Release Tablets Recalled by Ascend...

The Issue: Failed Dissolution Specifications: low out of specification results for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 22, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Triton Canister System (finished part numbers FG 12009 Recalled by Stryker...

The Issue: Some Canister Scanning Labels used to calibrate the Triton Canister System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2020· BioFire Diagnostics, LLC

Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...

The Issue: There is an increased risk of false positive Proteus results when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2020· BioFire Diagnostics, LLC

Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...

The Issue: There is an increased risk of false positive Proteus results when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2020· Braemar Manufacturing, LLC

Recalled Item: Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr....

The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2020· Braemar Manufacturing, LLC

Recalled Item: Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr....

The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...

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

Class II — Potential Health HazardOngoing
FoodJanuary 21, 2020· ABH Nature's Products, Inc.

Recalled Item: All Dietary Supplement manufactured and distributed by ABH Nature's Products...

The Issue: Firm ordered by consent decree to recall all products because the products...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: Columbus R/PS TIB.PLATEAU Cemented Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: COLUMBUS CRA/PSA TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: COLUMBUS CR/PS TIB.PLAT.PLASMAPORE Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: AS COLUMBUS CR/PS TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: COLUMBUS REV F TIBIA OFFSET CEMENTED Recalled by Aesculap Implant Systems...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Polymer Technology Systems, Inc.

Recalled Item: PTS Detect Cotinine Recalled by Polymer Technology Systems, Inc. Due to The...

The Issue: The firm is removing the product from the market after discussions with the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 20, 2020· Macleods Pharma Usa Inc

Recalled Item: Montelukast Sodium Chewable Tablets Recalled by Macleods Pharma Usa Inc Due...

The Issue: Failed Dissolution Specifications: testing revealed low out of specification...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 19, 2020· EHOB, Inc.

Recalled Item: Econocare Plus Overlay Item: 1025EC. Intended to aid in the Recalled by...

The Issue: Due to a nonconformance of product contamination (human blood) of Econocare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Beckman Coulter Inc.

Recalled Item: LabPro Data Management System Recalled by Beckman Coulter Inc. Due to A...

The Issue: A security-only update was released via remote diagnostics on January 14,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Ormco/Sybronendo

Recalled Item: SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due...

The Issue: The action is being taken due to an increase in complaints relating to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· COVIDIEN LLC

Recalled Item: Covidien Endo GIA Ultra Universal Stapler 12 mm-intended for resection...

The Issue: Potential for the sterile barrier to be compromised. Products with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Ormco/Sybronendo

Recalled Item: SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due...

The Issue: The action is being taken due to an increase in complaints relating to the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 16, 2020· Shandex Personal Care Manufacturing Inc.

Recalled Item: Walgreens Acne Cleansing Bar Recalled by Shandex Personal Care Manufacturing...

The Issue: Presence of Foreign Substance; Metal contaminant visible in product (screen...

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

Class II — Potential Health HazardOngoing
Refund