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. 2,488 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,488 in last 12 months

Showing 2128121300 of 49,990 recalls

DrugAugust 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-TESTOSTERONE CYP 200MG/ML MDV In SESAME OIL Recalled by First Royal Care...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 12, 2019· Zeus Scientific, Inc.

Recalled Item: ZEUS ELISA Parvovirus B19 IgM Test System Recalled by Zeus Scientific, Inc....

The Issue: FDA inspection identified that due to increased positivity (false positives)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2019· Varian Medical Systems, Inc.

Recalled Item: Varian Multileaf Collimator [MLC] Recalled by Varian Medical Systems, Inc....

The Issue: After a recent upgrade to the collimator software version 8.5, the firm...

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

Class II — Potential Health HazardOngoing
DrugAugust 9, 2019· Ridge Properties, LLC

Recalled Item: PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Liquid Gel...

The Issue: Microbial Contamination of Non-Sterile Products: products were found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2019· Ridge Properties, LLC

Recalled Item: Superior Pain & Itch Relief (lidocaine) Liquid Gel Recalled by Ridge...

The Issue: Superpotent Drug: products were found to be contaminated and above...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2019· Ridge Properties, LLC

Recalled Item: PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Cream Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: products were found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2019· Ridge Properties, LLC

Recalled Item: Soothing Sore Relief (lidocaine) Liquid Gel Recalled by Ridge Properties,...

The Issue: Superpotent Drug: products were found to be contaminated and above...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2019· Ridge Properties, LLC

Recalled Item: Soothing Sore Relief (lidocaine) Cream Recalled by Ridge Properties, LLC Due...

The Issue: Superpotent Drug: products were found to be contaminated and above...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2019· Ridge Properties, LLC

Recalled Item: Superior Pain & Itch Relief (lidocaine) Cream Recalled by Ridge Properties,...

The Issue: Superpotent Drug: products were found to be contaminated and above...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2019· American Health Packaging

Recalled Item: Carbamazepine Recalled by American Health Packaging Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 9, 2019· Medtronic Navigation, Inc.

Recalled Item: Medtronic Nexframe Stereotactic System and StealthStation Cranial software...

The Issue: Entry point and lead placement inaccuracies during deep brain stimulation...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Esthetic Abutment CC RP 1.5 mm pre-manufactured prosthetic components...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Temporary Abutment Engaging CC RP pre-manufactured prosthetic components...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Universal Base CC RP 1.5 mm Recalled by Nobel Biocare Usa Llc Due to...

The Issue: Packages of abutments (universal base) may contain an incorrect screw. While...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Temporary Snap Abutment Engaging CC RP 1.5 mm Recalled by Nobel Biocare Usa...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Temporary Abutment Non-Engaging CC RP pre-manufactured prosthetic components...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Nobel Biocare Usa Llc

Recalled Item: Snappy Abutment 5.5 CC RP 3 mm Recalled by Nobel Biocare Usa Llc Due to...

The Issue: Packages of abutments may contain an incorrect screw. While the screw will...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Randox Laboratories Ltd.

Recalled Item: Liquid Protein Calibrators (SP CAL (LIQ)) Catalogue Number: IT2691 GTIN:...

The Issue: The assigned value for Rheumatoid Factor over recovers against the material...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· Randox Laboratories Ltd.

Recalled Item: Rheumatoid Factor Standard (RF CAL) Catalogue Number: RF2301 GTIN:...

The Issue: The assigned value for Rheumatoid Factor over recovers against the material...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2019· GE Healthcare, LLC

Recalled Item: Proteus XR/a (SlOK : K993090) Recalled by GE Healthcare, LLC Due to...

The Issue: Intermittently not receiving an audible exposure indication upon completion...

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

Class II — Potential Health HazardOngoing