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 1740117420 of 48,770 recalls

DrugJuly 27, 2020· Calvin Scott & Company, Inc.

Recalled Item: Phentermine HCL White/Blue Speckled tablets Recalled by Calvin Scott &...

The Issue: CGMP Deviations: Light sensitive drug products repackaged in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2020· Calvin Scott & Company, Inc.

Recalled Item: Phendimetrazine Brown/Clear Capsules Recalled by Calvin Scott & Company,...

The Issue: CGMP Deviations: Light sensitive drug products repackaged in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2020· Calvin Scott & Company, Inc.

Recalled Item: Topiramate 25mg Tabs White/round tablets Recalled by Calvin Scott & Company,...

The Issue: CGMP Deviations: Light sensitive drug products repackaged in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 27, 2020· Office Depot Inc

Recalled Item: JINYINSHAN Recalled by Office Depot Inc Due to Test results revealed that...

The Issue: Test results revealed that the KN95 masks failed to filter greater than 95%...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· C.A. Greiner & Sohne Gesellschaftmbh

Recalled Item: Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Recalled by C.A....

The Issue: Sample leaking from the sleeve covering the needle inside the cannula

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 34cc IAB Kit...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible DCI Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 40cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 35cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-MEGA 8Fr 50cc IAB Kit P/N:...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Sensation Plus 8Fr 50cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 25cc IAB Kit...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 35cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-MEGA 7.5Fr 30cc IAB Recalled...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 40cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Karl Storz Endoscopy

Recalled Item: Flexible Intubation Video Endoscope Recalled by Karl Storz Endoscopy Due to...

The Issue: Updated sterilization instructions are being provided to ensure 1) a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2020· Datascope Corporation

Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 34cc IAB...

The Issue: Potential Endotoxin Contamination

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

Class II — Potential Health HazardOngoing