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 1552115540 of 48,770 recalls

DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Antiseptic Hand Cleaner (Chloroxylenol Recalled by Spartan Chemical Co Inc...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1%)...

The Issue: Microbial Contamination of Non-Sterile Products; lot tested positive for...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy Eucalyptus Mint Sanitizing Handwash (Benzalkonium Chloride...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿s3 - Product Recalled by Nobel Biocare...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s6 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Nobel Biocare Procera LLC

Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - Recalled by Nobel Biocare Procera...

The Issue: Not manufactured to specification

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Atos Medical AB

Recalled Item: Provox Life Night HME Recalled by Atos Medical AB Due to Provox Life Night...

The Issue: Provox Life Night HME may be incorrectly inserted sideways or forcefully...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for Recalled by...

The Issue: 3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75...

The Issue: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% may show...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2021· Philips North America Llc

Recalled Item: Philips Xper Flex Cardio (FC2010 Recalled by Philips North America Llc Due...

The Issue: Performance issues with the Xper Flex Cardio Physio Monitoring System...

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

Class II — Potential Health HazardOngoing
DrugMarch 26, 2021· Antoto-K

Recalled Item: Thumbs Up 7 Red 70K Recalled by Antoto-K Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 26, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Cefprozil for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 26, 2021· Sabra Dipping Company, LLC

Recalled Item: Sabra Dipping Co Recalled by Sabra Dipping Company, LLC Due to Potential...

The Issue: Potential Salmonella contamination

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 26, 2021· Radiometer Medical ApS

Recalled Item: PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized...

The Issue: Radiometer has become aware of an issue with PICO70 Arterial Blood Sampler....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· ROi CPS LLC

Recalled Item: Regard Dressing Change Tray Recalled by ROi CPS LLC Due to ChloraPrep...

The Issue: ChloraPrep applicators in the kit can grow organisms that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS¿ Black Slides CATALOG #: J02316 - Product Usage: Recalled by...

The Issue: Delayed results. Ortho confirmed that two lots of VITROS Black Slides are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number:...

The Issue: Some Artis zee ceiling systems show an increased abrasion of the cabling at...

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2021· S & B Story LLC

Recalled Item: Imperial Extreme 2000 Capsules Recalled by S & B Story LLC Due to Marketed...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund