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. 1,105 recalls have been distributed to Iowa in the last 12 months.
Showing 2521–2540 of 28,127 recalls
Recalled Item: Medline custom medical procedure kits labeled as: 1) MICRODISECTOMY PACK...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) MEM MAXILLOFACIAL...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...
The Issue: Software issues were identified in application version 2.x.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) VP SHUNT CDS Recalled...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...
The Issue: Software issues were identified in application version 2.x.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: DEEP BRAIN STIMULATION...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: See DocMan Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Custom...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) CERVICAL PACK-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216 Recalled by...
The Issue: The following four issues are included: 1. Certain Channel Settings may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Ketone Hospital Meter System. Model/Catalog Number: 63683....
The Issue: A software bug within the meter firmware leads to transmission of erroneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Hospital Meter System. Model/Catalog Number: 63685....
The Issue: A software bug within the Gen 2 StatStrip Hospital Meter firmware leads to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatStrip Glucose Ketone (mmol/L) Hospital Meter System. Model/Catalog...
The Issue: A software bug within the meter firmware leads to transmission of erroneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...
The Issue: Devices were identified as released after repair without full testing being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...
The Issue: Devices were identified as released after repair without full testing being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE SAFELINK Recalled by Greiner Bio-One GmbH Due to The VACUETTE...
The Issue: The VACUETTE SAFELINK Holder with male luer lock may leak blood due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 820 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tec 850 ISO Anesthesia Vaporizer Recalled by GE Medical Systems, LLC Due to...
The Issue: Due to a manufacturing issue, certain Tec 6 Plus and Tec 800 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.