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. 2,627 recalls have been distributed to Iowa in the last 12 months.
Showing 6581–6600 of 28,127 recalls
Recalled Item: KARL STORZ Radel Sterilization Trays Recalled by Karl Storz Endoscopy Due to...
The Issue: Plastic sterilization trays used to encase and protect medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NextSeq 550Dx Instrument Recalled by Illumina, Inc. Due to Cybersecurity...
The Issue: Cybersecurity vulnerability concerning the software used for sequencing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Toxicology Calibrator (TOX CAL)-The Atellica¿ CH Toxicology...
The Issue: Reassignment of the Atellica CH Toxicology Calibrators (TOX CAL) and ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry ToxAmmonia Calibrator- In vitro diagnostic use in the...
The Issue: Reassignment of the Atellica CH Toxicology Calibrators (TOX CAL) and ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraLife Autoclavable Double Swivel Elbow Recalled by Smiths Medical ASD...
The Issue: DuraLife devices instructions for cleaning and sterilization have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...
The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...
The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraLife Autoclavable Silicone Extension Tube Recalled by Smiths Medical ASD...
The Issue: DuraLife devices instructions for cleaning and sterilization have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraLife Autoclavable Silicone Extension Tube Recalled by Smiths Medical ASD...
The Issue: DuraLife devices instructions for cleaning and sterilization have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...
The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES (Med ES Main) Recalled by CareFusion 303, Inc. Due to...
The Issue: Automated dispensing cabinet software is experiencing: 1) ES device download...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Infinity M300 and M300+ Recalled by Draeger Medical Systems, Inc....
The Issue: The software on the Infinity CentralStation drops peaks on narrow waveforms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Infinity CentralStation (ICS) Recalled by Draeger Medical Systems,...
The Issue: The software on the Infinity CentralStation drops peaks on narrow waveforms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEO Instrument Kit for EPS Plate Recalled by GRAMERCY EXTREMITY ORTHOPEDICS...
The Issue: Instrument Kits for EPS plates may contain drill guides with incorrect drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pilot COVID-19 At-Home Test Recalled by SD Biosensor, Inc. Due to The liquid...
The Issue: The liquid buffer component in the affected test kit lots was determined to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA Recalled by Greiner Bio-One...
The Issue: Some of the tubes may be incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom pro+ mattress Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential for mattress cover damage (delamination) which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eye and Ear Dropper Recalled by Apothecary Products, LLC Due to Potential...
The Issue: Potential for glass dropper to have glass particulate on the outside surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicine Dropper Recalled by Apothecary Products, LLC Due to Potential for...
The Issue: Potential for glass dropper to have glass particulate on the outside surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs Recalled by...
The Issue: The case and each (i.e. packet) labels for the DYND3000xxP series do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.