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. 2,475 recalls have been distributed to Iowa in the last 12 months.
Showing 22381–22400 of 49,990 recalls
Recalled Item: Laxmi Brand Dried Apricot 7 oz (200g) Plastic Pouch Code: 2324617054...
The Issue: Product contains elevated levels of undeclared Sulfites
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Centricity Universal Viewer 6.0 Is a device that displays medical Recalled...
The Issue: There is the possibility of viewing studies directly from the Enterprise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Senographe Pristina - Product Usage: Senographe Pristina generates...
The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS Foundation Centricity PACS software product is intended for...
The Issue: There is the possibility of viewing studies directly from the Enterprise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Pristina Serena - Product Usage: Pristina Serena is an Recalled by GE...
The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 37cm Shaft PRODUCT CODE: NSLX137C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InterStim(TM) System Recalled by Medtronic Neuromodulation Due to There is a...
The Issue: There is a potential for an unexpected increase in stimulation during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 45cm Shaft PRODUCT CODE: NSLX145C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immulox Recalled by APS BioGroup, Inc Due to The recall is being conducted...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DPS Throat Spray Recalled by APS BioGroup, Inc Due to The recall is being...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Viralox Recalled by APS BioGroup, Inc Due to The recall is being conducted...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Immuno PRP Spray Recalled by APS BioGroup, Inc Due to The recall is being...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cool Haus Awesome Dessert - Dairy Free Horchata Frozen Dessert Recalled by...
The Issue: Product contains undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IntraClude Intra-Aortic Occlusion Device Recalled by Edwards Lifesciences,...
The Issue: Possibility of balloon rupture in intra-aortic occlusion devices. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer SST Part/Catalog No.365967 Recalled by Becton Dickinson &...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Z (No Additive Tubes) Part/Catalog No.365963 Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer PST Tubewith LH (Lithium Heparin) - Amber Part/Catalog...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MicrotainerTubes with K2E (K2EDTA) Catalog Number: 365974 Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Microtainer Tubes with FE (Sodium Fluoride / Disodium EDTA) Recalled by...
The Issue: Damaged reservoir may lead to a decreased fill volume causing samples to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.