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 1854118560 of 48,770 recalls

Medical DeviceMarch 17, 2020· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew FOOTPRINT Ultra PK Suture Anchor Recalled by Smith & Nephew,...

The Issue: Space between the device and the packaging permits excessive movement which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Rayner Intraocular Lenses Limited

Recalled Item: RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Recalled by Rayner...

The Issue: RaySert PLUS RSP01 LOT K030 labeled with an expiry of 2024-01 contained an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5 Part Number: 72202901...

The Issue: Space between the device and the packaging permits excessive movement which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Bard Peripheral Vascular Inc

Recalled Item: Jamshidi Bone Marrow Biopsy/Aspiration Needle Recalled by Bard Peripheral...

The Issue: Sterility compromised due to packaging pouches that may not be sealed properly

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

Class II — Potential Health HazardOngoing
DrugMarch 16, 2020· PharMEDium Services, LLC

Recalled Item: succinylcholine Chloride Recalled by PharMEDium Services, LLC Due to Firm is...

The Issue: Firm is recalling 46 lots of various products because of a lack of sterility...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2020· PharMEDium Services, LLC

Recalled Item: ePHEDrine Sulfate 5 mg per mL 25 mg per 5 mL Recalled by PharMEDium...

The Issue: Firm is recalling 46 lots of various products because of a lack of sterility...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2020· PharMEDium Services, LLC

Recalled Item: fentaNYL Citrate Injection Recalled by PharMEDium Services, LLC Due to Firm...

The Issue: Firm is recalling 46 lots of various products because of a lack of sterility...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2020· PharMEDium Services, LLC

Recalled Item: ePHEDrine Sulfate 10 mg per mL 50 mg per 5 Recalled by PharMEDium Services,...

The Issue: Firm is recalling 46 lots of various products because of a lack of sterility...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2020· PharMEDium Services, LLC

Recalled Item: fentaNYL Citrate 50 mcg per mL Recalled by PharMEDium Services, LLC Due to...

The Issue: Firm is recalling 46 lots of various products because of a lack of sterility...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2020· PharMEDium Services, LLC

Recalled Item: HYDROmorphone in 0.9% Sodium Chloride HCl Recalled by PharMEDium Services,...

The Issue: Firm is recalling 46 lots of various products because of a lack of sterility...

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

Class II — Potential Health HazardOngoing
Refund