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 17301–17320 of 28,127 recalls
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe and Hypodermic Needle Recalled by International Medsurg...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piston Syringe Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiLITE(TM) Products for Laser Surgery Recalled by Xintec Corp Due to It...
The Issue: It has been determined that the reprocessing instructions may not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Cardioplegia Adapter with Pressure Port Provides access for a Recalled...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GC80 Digital X-ray Imaging System Recalled by NeuroLogica Corporation...
The Issue: An image was obtained with over exposure during a Thorax examination using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Extension Line Adapters 20 in length Used to extend Recalled by...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pressure Disposable Pressure Display Sets Extends the pressure line...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION Recalled by Quidel Corporation Due...
The Issue: In-house testing revealed the presence of plastic spurs at the tips of some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pressure Monitoring Extension Line Adapters Extends the pressure line...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Antegrade/Retrograde Adapter Method for perfusion of cardioplegia...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Body Alignment Driver. 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: PALLAS M/MAXIMIS 350 Straight Rod. Part of MAXIMIS Pedicle Screw Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contiplex Nerve Block Tray. Product Catalog Number: 570205. Local anesthesia...
The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.