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. 2,590 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,590 in last 12 months

Showing 1222112240 of 28,127 recalls

Medical DeviceJanuary 22, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Triton Canister System (finished part numbers FG 12009 Recalled by Stryker...

The Issue: Some Canister Scanning Labels used to calibrate the Triton Canister System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2020· BioFire Diagnostics, LLC

Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...

The Issue: There is an increased risk of false positive Proteus results when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2020· BioFire Diagnostics, LLC

Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to There is an...

The Issue: There is an increased risk of false positive Proteus results when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2020· Braemar Manufacturing, LLC

Recalled Item: Braemar Manufacturing LLC DL950 Holter Monitor 1285 Corporate Center Dr....

The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2020· Braemar Manufacturing, LLC

Recalled Item: Braemar Manufacturing LLC DL900 Holter Monitor 1285 Corporate Center Dr....

The Issue: An issue with the DL900 and DL950 Series Holter Recorder was recognized on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: Columbus R/PS TIB.PLATEAU Cemented Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: COLUMBUS CRA/PSA TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: COLUMBUS CR/PS TIB.PLAT.PLASMAPORE Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: AS COLUMBUS CR/PS TIB.PLAT.CEMENTED Recalled by Aesculap Implant Systems LLC...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Aesculap Implant Systems LLC

Recalled Item: COLUMBUS REV F TIBIA OFFSET CEMENTED Recalled by Aesculap Implant Systems...

The Issue: Low Density Polyethylene (LDPE) particles may be present on the surface of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Polymer Technology Systems, Inc.

Recalled Item: PTS Detect Cotinine Recalled by Polymer Technology Systems, Inc. Due to The...

The Issue: The firm is removing the product from the market after discussions with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2020· Hologic, Inc.

Recalled Item: Selenia Dimensions Mammography System Recalled by Hologic, Inc. Due to The...

The Issue: The recalling firm has received reports from the field of the C-arm on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2020· EHOB, Inc.

Recalled Item: Econocare Plus Overlay Item: 1025EC. Intended to aid in the Recalled by...

The Issue: Due to a nonconformance of product contamination (human blood) of Econocare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2020· Kentec Medical, Inc

Recalled Item: Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes....

The Issue: Feeding tube plastic tethered closure cap may possibly fracture or break....

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

Class II — Potential Health HazardOngoing