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. 2,392 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,392 in last 12 months

Showing 2238122400 of 48,770 recalls

Medical DeviceMarch 21, 2019· Conmed Corporation

Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...

The Issue: Voids in the seal or a partial seal results in an open channel and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Conmed Corporation

Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...

The Issue: Voids in the seal or a partial seal results in an open channel and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Conmed Corporation

Recalled Item: ConMed Anchor Tissue Retrieval System" Recalled by Conmed Corporation Due to...

The Issue: Voids in the seal or a partial seal results in an open channel and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via syngo.CT Cardiac Function Recalled by Siemens Medical Solutions...

The Issue: There is a potential risk of a wrong measurement in the annulus plane during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via syngo.CT Cardiac Planning Recalled by Siemens Medical Solutions...

The Issue: There is a potential risk of a wrong measurement in the annulus plane during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics Due...

The Issue: Potential for sample fluid to be dispensed to an incorrect position on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Digital Linear Accelerators of type: ARTISTE MV System MEVATRON...

The Issue: Advisory issued not to disable or bypass the AMP function. Disabling or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2019· GETINGE US SALES LLC

Recalled Item: Maquet Servo-I Ventilator System -EDI CATHETER PHT Free 6Fr/49cm 5/pkg...

The Issue: Edi Catheter labeled with wrong expiry date on single pack EDI catheter boxes

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

Class III — Low RiskOngoing
DrugMarch 19, 2019· LUPIN SOMERSET

Recalled Item: Gavilyte-N Recalled by LUPIN SOMERSET Due to Labeling Not Elsewhere...

The Issue: Labeling Not Elsewhere Classified; orange and cherry flavor packets...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 19, 2019· Merical, LLC

Recalled Item: Walgreens Probiotic 12.5 Billion Active Cultures Recalled by Merical, LLC...

The Issue: Incorrect probiotic strain used in formulation which did not match product...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 19, 2019· GE Healthcare, LLC

Recalled Item: AIR Technology Anterior Array Recalled by GE Healthcare, LLC Due to The...

The Issue: The outer seam of the coil, closest to the system cable, may separate and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2019· Collagen Matrix, Inc.

Recalled Item: Neomem Resorbable Collagen Membrane Recalled by Collagen Matrix, Inc. Due to...

The Issue: Product was packaged in the wrong box; may have been placed inside a Neomem...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2019· Carestream Health, Inc.

Recalled Item: OnSight 3D Extremity System- X-Ray Recalled by Carestream Health, Inc. Due...

The Issue: When the user performs the re-assignment of a parent / companion pair, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2019· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Performance Series Sagittal Blade Recalled by Stryker Instruments Div. of...

The Issue: During manufacture, packaging materials for a small portion of the lot may...

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

Class II — Potential Health HazardOngoing
DrugMarch 18, 2019· Ingenus Pharmaceuticals Llc

Recalled Item: Diclofenac Sodium Topical Solution Recalled by Ingenus Pharmaceuticals Llc...

The Issue: Defective Container: firm discovered samples stored horizontally as well as...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 18, 2019· Ideal Implant Incorporated

Recalled Item: IDEAL IMPLANT Structured Breast Implant Recalled by Ideal Implant...

The Issue: The implants were deflating due to a piece of silicone disrupting the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to Continuous...

The Issue: Continuous operation at very high tube output may result in increased wear...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2019· Roche Diagnostics Corporation

Recalled Item: Albumin BCP Product Usage: ALBP is an in vitro test Recalled by Roche...

The Issue: The reagent lot is exhibiting calibration failures, QC imprecision, and...

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

Class II — Potential Health HazardOngoing
DrugMarch 15, 2019· Estee Lauder Inc

Recalled Item: Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15 Recalled...

The Issue: Defective container: Ineffective seal between the cap and jar of the...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2019· Pfizer Inc.

Recalled Item: Cleocin Phosphate Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

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

Class III — Low RiskOngoing
Refund