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. 1,069 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
1,069 in last 12 months

Showing 16241–16260 of 49,990 recalls

Medical DeviceMarch 19, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Interventional Fluoroscopic X-Ray System ARTIS icono biplane- 11327600 ARTIS...

The Issue: Siemens has become aware of a potential issue with software version VE20C....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2021· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer - Product Usage: intended to assist in the...

The Issue: When the Cross Enterprise Display option is enabled on the Centricity...

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

Class II — Potential Health HazardOngoing
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v...

The Issue: CGMP Deviations: Product is being recalled because at labeled storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% Recalled...

The Issue: Microbial Contamination of Non-Sterile Product:.Product is being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· X-Gen Pharmaceuticals Inc.

Recalled Item: Neomycin Sulfate Tablets Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Failed Stability Specifications: Out of Specification (OOS) result reported...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v...

The Issue: Microbial Contamination of Non-Sterile Product.Product is being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Hi-Lite Orange 2% w/v chlorhexidine gluconate (CHG) and...

The Issue: Non-sterility.Product is being recalled because at labeled storage...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear Recalled by CareFusion 213, LLC Due to...

The Issue: Non-sterility.Product is being recalled because at labeled storage...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Hi-Lite Orange 2% w/v chlorhexidine gluconate (CHG) and...

The Issue: Lack of Assurance of Sterility: Product is being recalled because at labeled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% Recalled...

The Issue: CGMP Deviations: Product is being recalled because at labeled storage...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 19, 2021· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear Recalled by CareFusion 213, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Product is being recalled because at labeled...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 18, 2021· Gentueri Inc

Recalled Item: Gentueri Viral Transport Medium (VTM) Recalled by Gentueri Inc Due to Medium...

The Issue: Medium showed visual turbidity and discoloration, potentially contaminating...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaBplus and AquaBplus B2 Water Purification System - Product Usage:...

The Issue: AquaBplus HF module on the AquaBplus 2500 osmosis system, an error in the US...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2021· Luminex Corporation

Recalled Item: VERIGENE Processor SP - Product Usage: intended for processing and Recalled...

The Issue: Potential for a false-negative result for Vibrio parahaemolyticus,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2021· Coltene Whaledent Inc

Recalled Item: Dental pins - TMS LINK PLUS Self-Threading Pins - Product Recalled by...

The Issue: The incorrect dental pins were packaged and subsequently distributed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Becton Dickinson & Co.

Recalled Item: BD BBL Martin-Lewis Agar Recalled by Becton Dickinson & Co. Due to Products...

The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Medtronic Sofamor Danek USA, Inc

Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...

The Issue: The shelf box identifies a small device actually contains a large device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Change Healthcare Enterprise Viewer Recalled by CHANGE HEALTHCARE CANADA...

The Issue: Change Healthcare has identified an intermittent software defect which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Medtronic Sofamor Danek USA, Inc

Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...

The Issue: The shelf box identifies a small device actually contains a large device,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2021· Becton Dickinson & Co.

Recalled Item: BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use Recalled by Becton...

The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...

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

Class II — Potential Health HazardOngoing