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. 2,447 recalls have been distributed to Iowa in the last 12 months.
Showing 27001–27020 of 28,127 recalls
Recalled Item: ABX PENTRA Creatinine 120 CP Recalled by Horiba Instruments, Inc dba Horiba...
The Issue: This recall was initiated because some customers were experiencing an alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic Fluoroscan Mini C-Arm Model with InSight2 Recalled by Hologic, Inc....
The Issue: InSight2, version 4.0 and 4.0.1 - DICOM images stored in PACS may be flipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic Fluoroscan Mini C-Arm Model with InSight- FD Software Version...
The Issue: Fluoroscan Mini C-Arm models -InSight2, version 4.0 and 4.0.1 - DICOM images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdvanDx GNR Traffic Light PNA FISH Recalled by Advandx Inc Due to GNR...
The Issue: GNR Traffic Light PNA Fish may have false positive results with Pseudomonas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gish 3/8 x 3/8" Straight Connector with Luer fitting Recalled by Sorin Group...
The Issue: Due to a molding irregularity, certain lots of connectors have the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gish 3/8 x 1/2" Reducer Connector with Luer fitting Recalled by Sorin Group...
The Issue: Due to a molding irregularity, certain lots of connectors have the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT Femoral Stem 12/14 Neck Taper Extended Offset Recalled by Zimmer, Inc....
The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501...
The Issue: Certain Samaritan 300/300P PAD devices may experience one or both of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trochar Scalpel Instrument (Surgical Punch) OrthoPediatrics intramedullary...
The Issue: A complaint received from sales representative that a replenishment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT Modular Stem Recalled by Zimmer, Inc. Due to Zimmer Inc. is initiating a...
The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT Hip System Femoral Stem Petite Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc. is initiating a removal of the CPT Modular Stem (item...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac...
The Issue: 3M determined that the electrical grounding mechanism for the Steri-Vac 5XL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Digital Diagnost with patient carriage Model: 712050 with serial...
The Issue: Hook does not securely hold the footplate in vertical position, causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Magnetom Skyra Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: When positioning the Flex Large 4 Coil (part No. 8625761) off-center in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The RIO (TGS 2.) Recalled by Mako Surgical Corporation Due to MAKO Surgical...
The Issue: MAKO Surgical Group recalled their RIO System software, version 2.4 and is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur BR Assay: Catalog Number: US: Recalled by Siemens...
The Issue: BR Assay for CA 27.29 Calibration Interval Change due quality control (QC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL M4735A Defibrillator/Monitors Recalled by Philips...
The Issue: HeartStart XL Defibrillator/Monitor (M4735A) used on a patient when AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Advanced Perfusion System 1 ASSEMBLY FLOW POD Product Usage: Recalled...
The Issue: Terumo Cardiovascular Systems (CVS) received two reports of the false back...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility...
The Issue: The potential exists for the wheel to rotate freely despite engagement of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Titanium Minimally Invasive Reduction Screw System Locking Cap...
The Issue: This action is being initiated following a detailed investigation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.