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. 2,492 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,492 in last 12 months

Showing 1518115200 of 48,770 recalls

FoodMay 5, 2021· Arizona Nutritional Supplements

Recalled Item: 365 Everyday Value Whey Protein Powder Natural Vanilla Flavor Recalled by...

The Issue: Whey Protein Powder was mistakenly packaged with Soy Protein Powder.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 5, 2021· Arcoma AB

Recalled Item: Omnera 400A Digital Radiographic System Recalled by Arcoma AB Due to There...

The Issue: There is the potential for the X-Ray system to short circuit due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Arcoma AB

Recalled Item: Omnera 400T Digital Radiographic System Recalled by Arcoma AB Due to There...

The Issue: There is the potential for the X-Ray system to short circuit due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Abbott Laboratories Inc. (St Jude Medical)

Recalled Item: v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris" System...

The Issue: Due to a software error, the user may lose functionality of the system or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Abbott Laboratories Inc. (St Jude Medical)

Recalled Item: WorkMate Claris v.1.2 Upgrade Kits Recalled by Abbott Laboratories Inc. (St...

The Issue: Due to a software error, the user may lose functionality of the system or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2021· Abbott Laboratories Inc. (St Jude Medical)

Recalled Item: v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris System...

The Issue: Due to a software error, the user may lose functionality of the system or...

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

Class II — Potential Health HazardOngoing
DrugMay 4, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities -Degradation Specifications:due to presence of ATV cyclo...

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

Class III — Low RiskOngoing
Refund
DrugMay 4, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Metformin HCl Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Presence of foreign substance: identified as activated carbon.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 4, 2021· bloommy Inc.

Recalled Item: "Bloomy*** Biotin Collagen Keratin***Capsules for SKIN Recalled by bloommy...

The Issue: Dietary supplement contains undeclared fish collagen

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 4, 2021· Simkins Brothers Sweets, LLC dba Natural Way Food Group

Recalled Item: Natural Way Almond Butter 16 oz. packaged in clear plastic jars Recalled by...

The Issue: Potential to contain undeclared peanuts

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 4, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer with Photometer Lamp (SMN 11075676) Siemens...

The Issue: Photometer Lamp May Reach Saturation Without Flagging Results, may generate...

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

Class II — Potential Health HazardOngoing
DrugMay 3, 2021· PFIZER, INC

Recalled Item: 0.5% Bupivacaine Hydrochloride Injection Recalled by PFIZER, INC Due to...

The Issue: Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 3, 2021· Mylan Institutional LLC

Recalled Item: Thiamine HCl Injection Recalled by Mylan Institutional LLC Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Cartons with the correct...

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

Class III — Low RiskOngoing
Refund
DrugMay 3, 2021· PFIZER, INC

Recalled Item: 1% Lidocaine HCl Injection Recalled by PFIZER, INC Due to Labeling: Label...

The Issue: Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 3, 2021· Pfizer Inc.

Recalled Item: Sterile Water for Inj. Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: particulate matter identified as an insect...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 3, 2021· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS CoV2 Ag calibrator (Product Code 6199950) - Product Usage: Recalled...

The Issue: Ortho investigated and confirmed the potential for unexpected failed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing