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 1136111380 of 48,770 recalls

Medical DeviceJuly 14, 2022· Roche Diagnostics Operations, Inc.

Recalled Item: cobas e801 Immunoassay Analyzer Recalled by Roche Diagnostics Operations,...

The Issue: Software issue resulting in signals and sample test results of Pre-Wash...

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

Class II — Potential Health HazardOngoing
DrugJuly 13, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Dr....

The Issue: FAILED DISSOLUTION SPECIFICATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 13, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Dr....

The Issue: FAILED DISSOLUTION SPECIFICATIONS

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 13, 2022· Pfizer Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of particulate matter: particulate identified as a beetle.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 13, 2022· Woodland Foods LLC

Recalled Item: Woodland Ingredients X06D Arborio Rice Recalled by Woodland Foods LLC Due to...

The Issue: possible presence of glass pieces

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 13, 2022· Albertsons Companies LLC

Recalled Item: Ready Meals Crab & Shrimp w/Ccktl SCE NET WT 12 Recalled by Albertsons...

The Issue: Undeclared allergens; fish, shellfish, egg, wheat, and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 13, 2022· Albertsons Companies LLC

Recalled Item: Ready Meals Snow Crab Legs Imitation Surimi SCE NET WT Recalled by...

The Issue: Undeclared allergens; fish, shellfish, egg, and wheat

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 13, 2022· Albertsons Companies LLC

Recalled Item: Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT Recalled by...

The Issue: Undeclared allergens; fish and shellfish

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 13, 2022· Shopaax.com

Recalled Item: Kingdom Honey Royal Honey VIP The Ultimate Power Source Recalled by...

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 13, 2022· Paragon 28, Inc.

Recalled Item: Grappler Suture Anchor Recalled by Paragon 28, Inc. Due to Suture anchor may...

The Issue: Suture anchor may break upon insertion, which could lead to potential debris...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2022· Materialise USA LLC

Recalled Item: ProPlan CMF Anatomical Model Recalled by Materialise USA LLC Due to...

The Issue: MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· FUJIFILM Healthcare Americas Corporation

Recalled Item: Surpria 64: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...

The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· FUJIFILM Healthcare Americas Corporation

Recalled Item: SCENARIA View: Software Version V1.08 Recalled by FUJIFILM Healthcare...

The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· FUJIFILM Healthcare Americas Corporation

Recalled Item: Surpria: Software Version V3.11 Recalled by FUJIFILM Healthcare Americas...

The Issue: Error 00003050 or 00003052 may occur during scanning, the captured images...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Sensis or Sensis Vibe Combo systems as follows: System Recalled by...

The Issue: The Sensis Signal Input Box provides hooks as a milled item on the bottom of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2022· Haimen Shengbang Laboratory Equipment Co. Ltd.

Recalled Item: HXBL/WETEX/Genesis Biomedical Viral Transport Container Recalled by Haimen...

The Issue: Distributed VTM outside of VTM Guidance and without clearance.

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

Class I — Serious Health HazardOngoing
DrugJuly 11, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Tacrolimus Ointment Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Defective Container: Tube split from side seam

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

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Ativan Injection (lorazepam injection Recalled by Hikma Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class II — Potential Health HazardOngoing
Refund