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. 2,460 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,460 in last 12 months

Showing 1610116120 of 48,770 recalls

DrugJanuary 11, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: Incorrect Labeling: Incorrect lot number on secondary packaging

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 11, 2021· C.R. Bard, Inc.

Recalled Item: Bard Clean-Cath Intermittent Catheter Recalled by C.R. Bard, Inc. Due to The...

The Issue: The device catheter tip was cut off (no tip) and the product packaging was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Ecolab Inc

Recalled Item: Slush + Warmer Disc Drape Recalled by Ecolab Inc Due to Slits were...

The Issue: Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Medtronic Neurosurgery

Recalled Item: Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA...

The Issue: Potential for variation in radiopaque marking visibility under radiographic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Medtronic Neurosurgery

Recalled Item: Medtronic PS Medical Cerebro Spinal Fluid (CSF)-Flow Control Valves for...

The Issue: Potential for variation in radiopaque marking visibility under radiographic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2021· Medtronic Neurosurgery

Recalled Item: Medtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control Valves for Recalled...

The Issue: Potential for variation in radiopaque marking visibility under radiographic...

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

Class II — Potential Health HazardOngoing
DrugJanuary 8, 2021· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Nortriptyline HCl Capsules Recalled by Taro Pharmaceuticals U.S.A., Inc. Due...

The Issue: CGMP deviations.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 8, 2021· Nihon Kohden America Inc

Recalled Item: WMTS Telemetry Receiver Recalled by Nihon Kohden America Inc Due to...

The Issue: Incorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2021· Cairn Diagnostics

Recalled Item: 13C-Spirulina Gastric Emptying Breath Test (GEBT) - Product Usage: intended...

The Issue: Potential for false negative diagnosis of gastroparesis. Certain GEBT kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2021· DePuy Orthopaedics, Inc.

Recalled Item: Universal Femoral Sleeves - Product Usage: used primarily in revision...

The Issue: The taper dimensions may be out of specification due to a production issue...

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

Class II — Potential Health HazardOngoing
DrugJanuary 7, 2021· Bausch Health Companies, Inc.

Recalled Item: Phytonadione Tablets 5mg Recalled by Bausch Health Companies, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications:Out of specification during the...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 7, 2021· Bausch Health Companies, Inc.

Recalled Item: Mephyton (phytonadione) Tablets 5mg Recalled by Bausch Health Companies,...

The Issue: Failed Impurities/Degradation Specifications:Out of specification during the...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 7, 2021· American Health Packaging

Recalled Item: Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals) Recalled by American...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 7, 2021· Baxter Healthcare Corporation

Recalled Item: The PrisMax System Version II Hemodialysis Delivery System: Automatic...

The Issue: Variability in the performance of the tubing in the ARPS (Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Lab Coats SMS X-Large Blue Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Kendall Spill Kit Recalled by Cardinal Health 200, LLC Due to Foreign Object...

The Issue: Gowns included in the kits potentially have rips, holes, tears, incomplete...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Gown Isolation W/Ties Xl Blue Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Gown Isolation W/Ties Univ Blu Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Drug Spill Kit-INSTI Recalled by Cardinal Health 200, LLC Due to...

The Issue: Gowns included in the kits potentially have rips, holes, tears, incomplete...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2021· Cardinal Health 200, LLC

Recalled Item: Lab Coats SMS 2X-Large White Recalled by Cardinal Health 200, LLC Due to...

The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...

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

Class II — Potential Health HazardOngoing