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. 2,489 recalls have been distributed to Iowa in the last 12 months.
Showing 20381–20400 of 49,990 recalls
Recalled Item: Genius 3 Tympanic Thermometer- electric thermometer Item Code: 303013...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer OEM Tympanic Item Code: 303063 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Anti-HAV IgM assay-for the in vitro qualitative detection of...
The Issue: Current software version of the Anti-HAV IgM APP-file (version 06.05-101)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 500 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 60 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 30 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 100 capsules Rx Only Recalled by...
The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% SODIUM CHLORIDE INJECTION Recalled by ICU Medical Inc Due to Presence...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LACTATED RINGER'S Injection Recalled by ICU Medical Inc Due to Presence of...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument - Product Usage: The...
The Issue: During the firm's review of May 2019 complaint data, a significant increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Knee Replacement System Model Number: TCR-111-1111-010102 -...
The Issue: Medial and lateral polyethylene inserts did not securely fit into the cobalt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taspen's Organics Respiratory Tea Recalled by Green Water, LLC Due to The...
The Issue: The products contain Coltsfoot, which is not to be used internally.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement Recalled...
The Issue: The products contain Coltsfoot, which is not to be used internally.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dragonfly Botanicals Full spectrum Breathe Deep 1000mg/oz Dietary Supplement...
The Issue: The products contain Coltsfoot, which is not to be used internally.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Python Embolectomy Catheters Recalled by Applied Medical Resources Corp Due...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical Dual Lumen Graft Cleaning Catheter & 1cc SYRINGE...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Embolectomy Catheter & 1 ml SYRINGE Recalled by Applied Medical...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene...
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide....
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rebel Monorail PtCr Coronary Stent System Recalled by Boston Scientific...
The Issue: Certain dilation and extension catheters are being recalled because these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.