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. 2,444 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,444 in last 12 months

Showing 3122131240 of 49,990 recalls

Medical DeviceJanuary 31, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: 882480: BrightView designed for single or dual detector nuclear imaging...

The Issue: Four issues: 1. Motion controller problem stops scan and no data image...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: 882482: BrightView XCT 882454 BrightView X upgrade to XCT Recalled by...

The Issue: Four issues: 1. Motion controller problem stops scan and no data image...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: 882478: BrightView X designed for single or dual detector nuclear Recalled...

The Issue: Four issues: 1. Motion controller problem stops scan and no data image...

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

Class II — Potential Health HazardOngoing
DrugJanuary 30, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Norethindrone Acetate and Ethinyl Estradiol Tablets Recalled by Mylan...

The Issue: Chemical Contamination: out of specification results for impurities were...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Tarina Fe 1/20 (Norethindrone Acetate and Ethinyl Estradiol Tablets Recalled...

The Issue: Chemical Contamination: out of specification results for impurities were...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 30, 2017· Actavis Inc

Recalled Item: Glipizide extended-release tablets Recalled by Actavis Inc Due to Failed...

The Issue: Failed Dissolution Specifications. Above out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 30, 2017· Bwi Inc

Recalled Item: Burts British Hand Cooked Potato Chips Sea Salt & Malted Recalled by Bwi Inc...

The Issue: Product is labeled as gluten free; however was labeled as containing an...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 30, 2017· Tearscience, Inc

Recalled Item: LipiFlow Thermal Pulsation System/LipiFlow Recalled by Tearscience, Inc Due...

The Issue: Labeling: The labeled storage temperature is not consistent with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2017· Beckman Coulter Inc.

Recalled Item: iChemVELOCITY Urine Chemistry System Recalled by Beckman Coulter Inc. Due to...

The Issue: The probe misalignment or bending has the potential to lead to delay in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2017· Hidrex GmbH

Recalled Item: Daavlin Aquex (DAAV1000) Recalled by Hidrex GmbH Due to The device was...

The Issue: The device was reclassified from a class III device to a class II device and...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 30, 2017· Hidrex GmbH

Recalled Item: Hidrex USA DVP1000 Recalled by Hidrex GmbH Due to The device was...

The Issue: The device was reclassified from a class III device to a class II device and...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 30, 2017· Hidrex GmbH

Recalled Item: Hidrex USA DP450 Recalled by Hidrex GmbH Due to The device was reclassified...

The Issue: The device was reclassified from a class III device to a class II device and...

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

Class III — Low RiskOngoing
DrugJanuary 27, 2017· Pharmedium Services, LLC

Recalled Item: Buffered Lidocaine Recalled by Pharmedium Services, LLC Due to Labeling;...

The Issue: Labeling; Label Mixup; outer packaging is incorrectly labeled as Buffered...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2017· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Mirtazapine Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablets...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 27, 2017· Batch International Llc

Recalled Item: Assorted chocolate truffles Recalled by Batch International Llc Due to The...

The Issue: The allergens such as soy, milk, almond, coconut, hazelnut, and/or wheat are...

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

Class III — Low RiskOngoing
Refund
FoodJanuary 27, 2017· Falafel King Ent, Inc.

Recalled Item: Falafel King Tzatziki Sauce. 10 ounce. Plastic container Recalled by Falafel...

The Issue: Falafel King announced a recall for their Tzatziki Sauce due to undeclared...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 27, 2017· Becton Dickinson & Company

Recalled Item: BD Vacutainer Sodium Polyanetholesulfonate 5.95 mg Sodium Chloride 14.4 mg...

The Issue: After a receiving a customer complaint for incorrect labeling, BD has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2017· National Biological Corp

Recalled Item: Hand Foot II Recalled by National Biological Corp Due to The wiring may...

The Issue: The wiring may allow the lamps to turn on with the key switch rather than...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2017· Maquet Cardiovascular, LLC

Recalled Item: VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage:...

The Issue: Maquet has received several complaints involving the VASOVIEW HEMOPRO...

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

Class II — Potential Health HazardOngoing
FoodJanuary 26, 2017· NSE Products, Inc.

Recalled Item: Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt. 1.59 Recalled...

The Issue: Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein...

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

Class I — Serious Health HazardOngoing
Refund