Product Recalls in Rhode Island

Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,434 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,434 in last 12 months

Showing 1700117020 of 27,456 recalls

Medical DeviceJune 16, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 100 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...

The Issue: The device failed to pump due to an electrical test failure code #58 (power...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 300 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...

The Issue: The device failed to pump due to an electrical test failure code #58 (power...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 15, 2017· Steris Corporation

Recalled Item: Vis-U-All High Temp 13"x18" 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 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· Steris Corporation

Recalled Item: Vis-U-All High Temp 4.5"x11" 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 5"x15" 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 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 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 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· 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· 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 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 3.5"x9" 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 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 7.5"x13" 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 Temperature Tubing 14"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 7.5"x13" 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 5"x15" 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