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. 1,794 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
1,794 in last 12 months

Showing 4196141980 of 49,990 recalls

FoodMay 28, 2014· Navitas, LLC., dba Navitas Naturals

Recalled Item: William & Sonoma Navitas Naturals brand Omega 3 Smoothie Mixer Recalled by...

The Issue: Data obtained from interviews of patients in a multistate outbreak of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 28, 2014· Navitas, LLC., dba Navitas Naturals

Recalled Item: Navitas Naturals Organic Sprouted Chia Powder Recalled by Navitas, LLC., dba...

The Issue: Data obtained from interviews of patients in a multistate outbreak of...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 27, 2014· Dot Foods Inc.

Recalled Item: Large Pitted Kalamata Olives Recalled by Dot Foods Inc. Due to This...

The Issue: This voluntary recall has been initiated because Savor Brands Large Pitted...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 27, 2014· Vascular Solutions, Inc.

Recalled Item: Langston Dual Lumen Catheters Recalled by Vascular Solutions, Inc. Due to...

The Issue: The inner catheter of some Langston V2 Dual Lumen Catheters have separated...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 27, 2014· BioFire Diagnostics, Inc.

Recalled Item: FirmArray Blood Culture Identification (BCID) Panel Recalled by BioFire...

The Issue: BioFire has identified an increased risk of false positive results when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension¿ Integrated Chemistry Systems intended to measure a variety of...

The Issue: There is a misassembly issue with the photometer installed on Dimension¿...

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

Class III — Low RiskOngoing
FoodMay 24, 2014· Interbake Foods Llc

Recalled Item: Mrs. Fields Milk Chocolate Chip Cookies Recalled by Interbake Foods Llc Due...

The Issue: Undeclared Walnuts. Some cartons labelled as Chocolate Chip cookies actually...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Flexible Aortic Arch Cannula 8.0mm with luer Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Soft-Flow Aortic Cannulae 6.0mm Recalled by Terumo Cardiovascular...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Venoatrial Cannulae 36/46 Fr with 1/2" flare or connector Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo TenderFlow Pediatric Venous Cannulae Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Soft-Flow Extended Aortic Cannulae 7.0mm & 8.0mm with or Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Soft-arc Aortic Cannula 8.0mm curved tip Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Three-stage Venous Return Cannulae 28 Fr with 3/8" flare Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Zimmer, Inc.

Recalled Item: Zimmer M/L Taper Reduced Neck Standard & Extended Offset Recalled by Zimmer,...

The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Measurement Clinical Chemistry System RAPIDPoint 500...

The Issue: RAPIDPoint 500 Measurement Cartridges may have an error code one or more...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Zimmer, Inc.

Recalled Item: Zimmer M/L Taper Hip Stem Standard & Extended Offset Recalled by Zimmer,...

The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns D4 Aortic Arch Cannulae 6.0mm Recalled by Terumo Cardiovascular...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing