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. 2,533 recalls have been distributed to Iowa in the last 12 months.
Showing 17461–17480 of 28,127 recalls
Recalled Item: PALLAS M/MAXIMIS MIS Screw 6.5 x 35mm. Part of MAXIMIS Recalled by Valorem...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Poly Screw 7.5 x 40mm. Part of MAXIMIS Recalled by Valorem...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Small Crosslink. Part of MAXIMIS Pedicle Screw Spinal...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Driver Shaft (5Hex Recalled by Valorem Surgical LLC Due to...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Tapper 5.5. Part of MAXIMIS Pedicle Screw Spinal Recalled...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Poly Screw 7.5 x 55mm. Part of MAXIMIS Recalled by Valorem...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS MIS Screw 5.5 x 50mm and 5.5 x Recalled by Valorem Surgical...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS 5.5 x 05mm Curved Rod. Part of MAXIMIS Recalled by Valorem...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Poly Screw 5.5 x 30mm. Part of MAXIMIS Recalled by Valorem...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Anti Torque. Part of MAXIMIS Pedicle Screw Spinal Recalled...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Open Extension (Small). Part of MAXIMIS Pedicle Screw...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ(R) Oncology Information System Recalled by Elekta, Inc. Due to...
The Issue: Retention of Outdated Information in an Order Set. In the Care Plan Library,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Unit Abutment Angled Recalled by Keystone Dental Inc Due to Abutments...
The Issue: Abutments are unable to accept the final abutment screw
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...
The Issue: The firm has identified that a fitting in some Slidemaker Stainer units may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Biomedical Stat Profile Prime Analyzer as follows: PN 52855 Recalled by...
The Issue: Software- scheduled A-QC analysis could initiate prior to a patient result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets...
The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary Recalled by ConMed...
The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nussloch GmbH ASP6025 Tissue Processor Recalled by Leica Microsystems, Inc....
The Issue: Incorrect labeling for specified voltage for the Alarm Connectors on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 300 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.