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. 2,618 recalls have been distributed to Iowa in the last 12 months.
Showing 10181–10200 of 28,127 recalls
Recalled Item: TECNIS Toric 1-Piece IOL Recalled by Johnson & Johnson Surgical Vision Inc...
The Issue: Due to the release of nonconforming Intraocular Lenses (IOLs).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis / Sensis Vibe systems with software version VD12 and Recalled by...
The Issue: System may sporadically freeze (lock-up) during operation or while being in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gram-Negative Bacteria And Associated Resistance Markers Recalled by BioFire...
The Issue: The firm has identified an increased risk of false positive Pseudomonas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire BCID2 Panel Recalled by BioFire Diagnostics, LLC Due to The firm has...
The Issue: The firm has identified an increased risk of false positive Pseudomonas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 Recalled by Corin Ltd...
The Issue: The size indicated on the labeling on the outer packaging, on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Recalled by Corin...
The Issue: The size indicated on the labeling on the outer packaging, on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RNA MEDICAL Recalled by Medline Industries Inc Due to Product was...
The Issue: Product was compromised during shipment.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digitial Medica X-ray Imagining System Recalled by Shanghai United Imaging...
The Issue: There is a potential for the X-Ray tube head (Touch screen interface) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular...
The Issue: Test results from the manufacturing line found a piece of damaged o-ring in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Band Recalled by G & H Wire Company Due to The text on the patient pack is...
The Issue: The text on the patient pack is correct and the product itself remains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible...
The Issue: The affected Milex Gellhorn pessaries were incorrectly manufactured with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions Ethicon Endo-Surgery Recalled by Stryker...
The Issue: Product was distributed without receiving regulatory clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various reprocessed products: PROVISION Recalled by ReNovo, Inc. Due to...
The Issue: Non-sterile product was shipped to customers labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator Single-Use Polypectomy Snares Recalled by Boston Scientific...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator II Single-Use Polypectomy Snares Outer box UPN Recalled by Boston...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AntIbody to SARS-CoV-2 - Product Usage: (Colloidal Gold) for IgG/IgM...
The Issue: Distributed COVID test kits without emergency use authorization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tube Tracheostomy and Tube Cuff Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Smiths Medical became aware that three lot numbers of a specific model of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 6F Launcher Guide Catheter 100cm EBU 3.75 Model Number: LA6EBU375...
The Issue: Sterility may be compromised due to an unsealed pouch
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.