Product Recalls in North Dakota
Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,461 recalls have been distributed to North Dakota in the last 12 months.
Showing 16961–16980 of 27,512 recalls
Recalled Item: Customer Epidural Anesthesia Tray. Product Catalog Number: 555234. 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: Pencan Spinal Needle Tray. Product Catalog Number: 333865. 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.
Recalled Item: Pain Management Tray. Product Catalog Number: 560602. Local anesthesia of...
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: 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.
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: PALLAS M/MAXIMIS MIS Screw5.5 x 55mm. 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 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 40mm Rod. 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 60mm 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 40mm 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 5.5 x 35mm 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 50mm Curved and precontoured Rod. Part of MAXIMIS 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 Guide Wire. 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 MIS 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 Distractor. 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: PALLAS M/MAXIMIS MIS Pedicle Cut. 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 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 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 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 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.