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 28861–28880 of 49,990 recalls
Recalled Item: PALLAS M/MAXIMIS MIS 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 Persuader. Part of MAXIMIS Pedicle Screw Spinal Fixation...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perifix FX Epidural Anesthesia Tray. Product Catalog Numbers: 551993...
The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perifix Single Dose Epidural Anesthesia Tray. Product Catalog Number:...
The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENCAN Spinal Anesthesia Tray. Product Catalog Number: 560590. Local...
The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS MISS/MIS Tapper 7.5 mm. Part of MAXIMIS Pedicle 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: PALLAS M/MAXIMIS Awl. Part of MAXIMIS Pedicle Screw Spinal Fixation Recalled...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perifix Epidural AnesthesiaTray. Product Catalog Numbers: 551879 Recalled by...
The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Cross Link Torque Handle. Part of MAXIMIS Pedicle 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 MIS Screw 6.5 x 45mm and 6.5 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 Poly Screw 5.5 x 50mm and 5.5 x 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 55mm MIS 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: PALLAS M/MAXIMIS MIS Screw 6.5 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 Poly Screw Driver B. Part of MAXIMIS 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: PALLAS M/MAXIMIS MISS/MIS Compressor and Rod Tightener. Part of MAXIMIS...
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 C. Probe. Part of MAXIMIS Pedicle Screw Spinal 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: PALLAS M/MAXIMIS Poly 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 6.5 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 60mm Curved 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: PALLAS M/MAXIMIS Poly Screw 7.5 x 45mm. 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.