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. 2,437 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,437 in last 12 months

Showing 1726117280 of 27,655 recalls

Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 3"x8" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 10.5"x28" Self Seal Pouch 100 pouches per box Recalled...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 8"x16" Heat Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 4"x100'. One roll per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 5.5"x10" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 10"x15" Heat Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Custom Assemblies Inc

Recalled Item: Various custom surgical kits manufactured for CMS Recalled by Custom...

The Issue: The firm manufactured and distributed custom surgical kits which contained...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· ICU Medical Inc

Recalled Item: Plum 360 Infusion System Recalled by ICU Medical Inc Due to Potential for...

The Issue: Potential for the Connectivity Engine Module of the affected unit to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 9"x100'. One roll per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 3.5"x22" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 6"x10" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 13"x18" Heat Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 18"x22" Self Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 18"x22" Heat Seal Pouch 100 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 7.5"x13.5" Heat Seal Pouch 200 pouches per box Recalled...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 6"x100'. One roll per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 4"x8" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2017· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: ArjoHuntleigh Flowtron ACS900 Recalled by Arjo, Inc. dba ArjoHuntleigh Due...

The Issue: Reports of the device failure involving delivering continuous pressure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2017· Cyberonics, Inc

Recalled Item: VNS Therapy¿ AspireHC¿ Generator Recalled by Cyberonics, Inc Due to...

The Issue: Manufacturing process used to assemble the circuit board may result in some...

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

Class II — Potential Health HazardOngoing