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 1778117800 of 28,127 recalls

Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: SV40 (MRQ-4) 0.5 ml catalog number 351 M-15. Microbiology - Recalled by Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· GE Healthcare, LLC

Recalled Item: Infant Warmer System (IWS) Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: HHV-8 (13810) Recalled by Cell Marque Corporation Due to Cell Marque has...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2017· Cell Marque Corporation

Recalled Item: Adenovirus (20/11 & 2/6) Recalled by Cell Marque Corporation Due to Cell...

The Issue: Cell Marque has determined the need to issue a product recall after...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2017· Philips Electronics North America Corporation

Recalled Item: NMT Patient Cable (989803174581) in use with lntelliVue NMT Module Recalled...

The Issue: Manufacturing defect may cause localized heating, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: CUSTOM SUTURE PACK Recalled by Medtronic Due to Potential for an incomplete...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. POLYSORB: POLSORB 0 18 U/D PRECUT 126R Recalled by Medtronic Due to...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. MAXON: MAXON 4/0 5X18" GREEN CV-24 D-TACH Recalled by Medtronic Due...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: USPACK-SUTURE KIT Recalled by Medtronic Due to Potential for an incomplete...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. BIOSYN: BIOSYN 4/0 18" VIOLET CV-25 DT Recalled by Medtronic Due to...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Cook Inc.

Recalled Item: OptiLite Multi-Use Holmium Laser Fibers Recalled by Cook Inc. Due to Cook...

The Issue: Cook Inc. is initiating a voluntary recall of the OptiLite Multi-Use Holmium...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Best Practice Kit Recalled by Medtronic Due to Potential for an incomplete...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: Sutures. ENDO STITCH: ENDO STITCH POLYSORB 0 48" U/D DLU SU Recalled by...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2017· Medtronic

Recalled Item: SCHRITTMACHER ANGIO X3 Recalled by Medtronic Due to Potential for an...

The Issue: Potential for an incomplete seal on the inner package, which may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD Recalled by...

The Issue: Implant Direct Sybron Manufacturing is recalling the Legacy Full-Contour...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: LapSac Introducer Recalled by Cook Inc. Due to COOK Medical is initiating a...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Circadiance LLC

Recalled Item: SmartMonitor 2 PS/PSL Recalled by Circadiance LLC Due to Circadiance has...

The Issue: Circadiance has determined that it is possible for certain Smart Monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Willscher Vas Reapproximator Set Recalled by Cook Inc. Due to COOK Medical...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Endoscopic Curved Needle Recalled by Cook Inc. Due to COOK Medical is...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Willscher Vas Reapproximator Plate Recalled by Cook Inc. Due to COOK Medical...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing