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. 2,518 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,518 in last 12 months

Showing 1108111100 of 48,770 recalls

Medical DeviceAugust 9, 2022· Technomed Europe

Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...

The Issue: Burns of varying degrees can occur to patients with electrodes left in while...

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2022· Akorn, Inc

Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc Due to...

The Issue: Identification of an unknown impurity at the 12-month stability point....

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2022· LNK International, Inc.

Recalled Item: Nighttime Sleep-Aid (doxylamine succinate HCl) tablets Recalled by LNK...

The Issue: Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as...

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2022· Baxter Healthcare Corporation

Recalled Item: Acetaminophen Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Temperature Abuse: Product distributed in trucks with labels attached to...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 3, 2022· Eclectic Institute Inc

Recalled Item: Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement Recalled by...

The Issue: Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 3, 2022· Wright Medical Technology, Inc.

Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...

The Issue: The outer label does not match the device inside the package. The affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· Wright Medical Technology, Inc.

Recalled Item: stryker EVOLVE Recalled by Wright Medical Technology, Inc. Due to The outer...

The Issue: The outer label does not match the device inside the package. The affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER Recalled by MEDLINE...

The Issue: Potential for the suction catheter to come apart from the green connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by...

The Issue: Potential for the suction catheter to come apart from the green connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by MEDLINE...

The Issue: Potential for the suction catheter to come apart from the green connector...

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

Class II — Potential Health HazardOngoing
DrugAugust 2, 2022· HERON THERAPEUTICS, INC.

Recalled Item: Zynrelef (bupivacaine and meloxicam) Recalled by HERON THERAPEUTICS, INC....

The Issue: Defective Delivery System: An incorrect 10 mL (12 mL) Luer (slip) syringe...

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

Class III — Low RiskOngoing
Refund
DrugAugust 2, 2022· CIPLA

Recalled Item: Difluprednate Ophthalmic Emulsion 0.05% Recalled by CIPLA Due to Lack of...

The Issue: Lack of Assurance of Sterility: Complaints received of defective container...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 2, 2022· Carwild Corporation

Recalled Item: FABCO ORS DENTAL ROLLS Recalled by Carwild Corporation Due to Sterility with...

The Issue: Sterility with new cotton source not validated

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

Class II — Potential Health HazardOngoing
DrugAugust 1, 2022· Akorn, Inc

Recalled Item: PrednisoLONE Oral Solution USP Recalled by Akorn, Inc Due to Defective...

The Issue: Defective Container: Product has incomplete induction seals.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 1, 2022· Randox Laboratories Ltd.

Recalled Item: The Randox Serology I Positive Control contains the following analytes...

The Issue: ***Update** :HBsAg analyte is also Non-Reactive on the Ortho Vitros analyser...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 6.5 IN (17 cm) APPX 0.78 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: MicroClave Clear Neutral Connector Recalled by ICU Medical, Inc. Due to Due...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 6" (15 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: MicroClave Clear Neutral Connector. A bidirectional connector used as an...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2022· ICU Medical, Inc.

Recalled Item: 8.5" (22 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...

The Issue: Due to a manufacturing defect which results in a visible gap between the...

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

Class II — Potential Health HazardOngoing