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. 2,562 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,562 in last 12 months

Showing 11411160 of 48,770 recalls

Medical DeviceSeptember 30, 2025· IMPRIS Imaging Inc

Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...

The Issue: There is a potential safety issue associated with the magnet venting paths...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis Pro MedStation Main Recalled by CareFusion 303, Inc. Due to...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: Various models of BD Pyxis MedFlex Recalled by CareFusion 303, Inc. Due to...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: Various models of BD Pyxis Pro 7-Drawer Auxiliary Recalled by CareFusion...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· IMPRIS Imaging Inc

Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...

The Issue: There is a potential safety issue associated with the magnet venting paths...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2025· IMPRIS Imaging Inc

Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...

The Issue: There is a potential safety issue associated with the magnet venting paths...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: All Serial Numbers/BD Pyxis CII Safe ES Tower Main Recalled by CareFusion...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· CareFusion 303, Inc.

Recalled Item: Various models of BD Pyxis Medbank: numbers: 1137-00 1145-00 Recalled by...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2025· B BRAUN MEDICAL INC

Recalled Item: Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET...

The Issue: The potential for micro-air bubbles observed in the bloodline and...

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

Class I — Serious Health HazardOngoing
DrugSeptember 29, 2025· Medline Industries, LP

Recalled Item: Medline Recalled by Medline Industries, LP Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Acella Pharmaceuticals, LLC

Recalled Item: Doxycycline Hyclate Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Failed dissolution specifications: Stability testing found that the lot did...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Acuity Specialty Products, Inc.

Recalled Item: AFCO Recalled by Acuity Specialty Products, Inc. Due to cGMP deviations: The...

The Issue: cGMP deviations: The recall was initiated because required receipt testing...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2025· Acuity Specialty Products, Inc.

Recalled Item: Wyandotte Recalled by Acuity Specialty Products, Inc. Due to cGMP...

The Issue: cGMP deviations: The recall was initiated because required receipt testing...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 26, 2025· MAYEJ COMERCIALIZADORA S. de R.L. de C.V.

Recalled Item: Italian Parsley packaged in 24lb boxes Recalled by MAYEJ COMERCIALIZADORA S....

The Issue: pathogen Cyclospora cayetanensis

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2025· Dr. Reddy's Laboratories, Inc.

Recalled Item: Succinylcholine Chloride Injection Recalled by Dr. Reddy's Laboratories,...

The Issue: Out-of-Specification (OOS) result during the 6-month stability testing;...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL End Caps for SAFE-T-FILL Blood Gas Capillaries Recalled by ASP...

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL MicroHematocrit Capillary Tubes Recalled by ASP Global, LLC. dba...

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· ASP Global, LLC. dba Anatomy Supply Partners, LLC.

Recalled Item: SAFE-T-FILL Micro Capillary Blood Collection Recalled by ASP Global, LLC....

The Issue: Due to products manufactured under an inadequate quality system to include...

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

Class II — Potential Health HazardOngoing