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. 2,499 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,499 in last 12 months

Showing 1258112600 of 48,770 recalls

Medical DeviceMarch 25, 2022· Medtronic formerly Covidien

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Medtronic formerly...

The Issue: The audible alarm may not sound and/or the omni-directional LED visual alarm...

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

Class I — Serious Health HazardOngoing
DrugMarch 24, 2022· Preferred Pharmaceuticals, Inc.

Recalled Item: Diclofenac Sodium Topical Solution 1.5% w/w Recalled by Preferred...

The Issue: CGMP Deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 24, 2022· Wilton Industries Inc

Recalled Item: Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit Recalled by Wilton...

The Issue: Milk is missing from the product's allergen Contains statement

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 24, 2022· Microbiologics Inc

Recalled Item: Inactivated macrolide and quinolone-resistant Mycoplasma genitalium Recalled...

The Issue: QC process was not adequate for the specification range.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2022· Abbott

Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...

The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2022· Abbott

Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...

The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...

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

Class II — Potential Health HazardOngoing
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE/ ANASTROZOLE *GS* OIL (10ML) 200MG/0.5MG/ML Recalled...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: GONADORELIN (5ML) 0.2 MG/ML INJECTABLE Recalled by Drug Depot, Inc., dba APS...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE/ DHEA *GS* 200/10MG/ML Injectable Recalled by Drug...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE/PROPIONATE *SES* Oil (10 ML) 160MG/20MG/ML Injectable...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Dissolution Specifications; during long term stability testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE *GS* (2 mL) 80 MG/ML Injectable Recalled by Drug...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE *GS* Oil 200 MG/ML Injectable Recalled by Drug Depot,...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Lansoprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed Dissolution Specifications; during long term stability testing.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE/ANASTROZOLE *GS* OIL 200MG/1MG/ML Injectable Recalled...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: (CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE Recalled by Drug Depot, Inc.,...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 23, 2022· Medtronic Vascular, Inc.

Recalled Item: Medtronic IN.PACT AV Recalled by Medtronic Vascular, Inc. Due to Packaging...

The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2022· Medtronic Vascular, Inc.

Recalled Item: Medtronic IN.PACT Admiral Recalled by Medtronic Vascular, Inc. Due to...

The Issue: Packaging for Balloon Catheters may be damaged resulting in loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2022· Sight Sciences, Inc.

Recalled Item: TearCare version 1.0 SmartHubs Recalled by Sight Sciences, Inc. Due to...

The Issue: Ophthalmic devices distributed prior to the recently-obtained 510(k)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· Steris Corporation

Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5 Recalled by Steris...

The Issue: Product not approved for release for US distribution

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

Class II — Potential Health HazardOngoing