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. 2,503 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,503 in last 12 months

Showing 1144111460 of 27,512 recalls

Medical DeviceJune 5, 2020· Verathon, Inc.

Recalled Item: GlideScope Core OneTouch Smart Cable Recalled by Verathon, Inc. Due to When...

The Issue: When video laryngoscopy system users apply, twisting motions while...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2020· OrthoPediatrics Corp

Recalled Item: OrthoPediatrics ACL Reconstruction System ShieldLoc 6mm implant component...

The Issue: ShieldLoc implant component of the ACL Reconstruction Systemlots may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Calibrator Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Calibration errors have been observed with the Total and Direct Bilirubin...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Chemistry Calibrator Recalled by Siemens Healthcare Diagnostics,...

The Issue: Calibration errors have been observed with the Total and Direct Bilirubin...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· HF Acquisition Co., LLC

Recalled Item: STAT KIT Model 550AI Emergency Medical Kit. P/N: 1010830 containing Recalled...

The Issue: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· HF Acquisition Co., LLC

Recalled Item: STAT KIT Model 550 Emergency Medical Kit P/N: 1009580 containing Recalled by...

The Issue: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· HF Acquisition Co., LLC

Recalled Item: STAT KIT Recalled by HF Acquisition Co., LLC Due to Instead of 2 doses,...

The Issue: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· HF Acquisition Co., LLC

Recalled Item: HealthFirst Emergency Medical Kit Recalled by HF Acquisition Co., LLC Due to...

The Issue: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Boston Scientific Corporation

Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...

The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Cardinal Health 200, LLC

Recalled Item: Cardinal Health NPWT Canister with Gel 300cc Recalled by Cardinal Health...

The Issue: Canisters potentially contain an oversized O-ring that cannot be installed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2020· Cardinal Health 200, LLC

Recalled Item: Cardinal Health NPWT Occlusion Detection Canister 300cc Recalled by Cardinal...

The Issue: Canisters potentially contain an oversized O-ring that cannot be installed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing