Product Recalls in Iowa

Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,533 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,533 in last 12 months

Showing 1748117500 of 28,127 recalls

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

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

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· Keystone Dental Inc

Recalled Item: Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant...

The Issue: An 8mm diameter bone tap was laser marked as 7mm diameter and was packed...

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· 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 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 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 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 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 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 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"x13.5" 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· 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 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 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 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 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 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 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 3.5"x22" 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 10.5"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