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. 2,447 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,447 in last 12 months

Showing 2902129040 of 49,990 recalls

Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Sorter 9tray Recalled by Tosoh Bioscience Inc Due to This recall has...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Automated Enzyme Immunoassay Analyzer AIA-900 Recalled by Tosoh...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Sorin Group USA, Inc.

Recalled Item: Sorin Group Aortic Arch Cannula Recalled by Sorin Group USA, Inc. Due to...

The Issue: Identification of excess plastic on the tip of the cannula.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe Recalled by Natus Neurology Inc...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Penumbra Inc.

Recalled Item: Penumbra 3D Revascularization Device It is indicated for used in Recalled by...

The Issue: Penumbra has identified an issue in these four lots involving a raw material...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 5 MHz Vascular Probe Recalled by Natus Neurology Inc Due to...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Natus Neurology Inc

Recalled Item: Nicolet¿ Elite¿ 3 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...

The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...

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

Class II — Potential Health HazardOngoing
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin 1 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma Inc....

The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma...

The Issue: Subpotent Drug: found to be below the specification for labeled assay.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin 100 mcg/mL QS 5% Dextrose Inj Recalled by Advanced Pharma Inc....

The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin (2 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma...

The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin (1 mg/5 mL) 1 mg in 5% Dextrose Inj Recalled by Advanced...

The Issue: Subpotent Drug: found to be below the specification for labeled assay.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin (1 mg/5 mL) 1 mg in 5% Dextrose Inj Recalled by Advanced...

The Issue: Stability Data Does Not Support Expiry: lots do not have stability that...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 9, 2017· Advanced Pharma Inc.

Recalled Item: NitroGlycerin 1 mg/10 mL in 5% Dextrose Inj Recalled by Advanced Pharma Inc....

The Issue: Subpotent Drug: found to be below the specification for labeled assay.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodJune 9, 2017· High Liner Foods Inc.

Recalled Item: HFS 1/20 Oven Ready Crunchy Sweet Potato Alaska Pollock Nuggets 1 oz....

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund