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. 2,546 recalls have been distributed to Iowa in the last 12 months.
Showing 16101–16120 of 28,127 recalls
Recalled Item: Straumann¿ Emdogain 0.15 ml 5-Pack. Enamel Matrix Derivative. Article Number...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.3 ml Multipack. Enamel Matrix Derivative. Article...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic ZEVO(TM) Anterior Cervical Plate System SLOT SCREW Recalled by...
The Issue: Slot screw had an overall length of 15mm, but per the specification, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann¿ Emdogain 0.7 ml Multipack USA. Enamel Matrix Derivative. Article...
The Issue: A change regarding the shelf life of a raw material was implemented without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E95 ultrasound system Product The device is intended Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LOGIQ E9 ultrasound system Product Usage: The device is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E90 ultrasound system Product Usage: Vivid E80 / Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E7 ultrasound system Product Usage: Vivid E7 is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Lithium Heparin Green Top Tube Recalled by Becton Dickinson &...
The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ EDTA Pink Top Tube Recalled by Becton Dickinson & Company Due...
The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ EDTA Tan Top Tube Recalled by Becton Dickinson & Company Due...
The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE LOGIQ 9 ultrasound system Product Usage: The device is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 Recalled...
The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E9 ultrasound system Product Usage: GE Vivid E9 Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E80 ultrasound system Vivid E80 / E90 / Recalled by GE Medical...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid 7 ultrasound system Product Usage: Vivid E7 is Recalled by GE...
The Issue: The system side of the power cord may break and expose the electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draco Enzymatic Deep-Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Recalled...
The Issue: Medline notified BMD that the Aplicare Povidone Iodine (PVP-I) Prep Pads...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.