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. 2,535 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,535 in last 12 months

Showing 73817400 of 27,512 recalls

Medical DeviceNovember 1, 2022· Cardinal Health

Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm) Recalled by...

The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2022· Cardinal Health

Recalled Item: Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter Recalled...

The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2022· Alcon Research, LLC

Recalled Item: Alcon Custom Pak Surgical Procedure Pack Recalled by Alcon Research, LLC Due...

The Issue: Due to difficulty removing the liner on the adhesive components of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2022· GE Medical Systems, LLC

Recalled Item: Centricity Universal Viewer 6.0. Used to display medical images (Including...

The Issue: There is the potential that after installation of the IAS tool, some studies...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2022· GE Medical Systems, LLC

Recalled Item: Centricity PACS-IW with Universal Viewer version 5.0. Used to display...

The Issue: There is the potential that after installation of the IAS tool, some studies...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2022· Southmedic, Inc.

Recalled Item: Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE Recalled by...

The Issue: Upon review of its batch record, Southmedic identified that lot # W92761 was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic...

The Issue: Confirmed an average positive bias of 40% for testosterone concentrations of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2022· Whele LLC DBA Perch

Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...

The Issue: The products may have the potential to burn customers. Firm has received...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2022· Whele LLC DBA Perch

Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...

The Issue: The products may have the potential to burn customers. Firm has received...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2022· Whele LLC DBA Perch

Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...

The Issue: The products may have the potential to burn customers. Firm has received...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2022· Trackx Technology Inc

Recalled Item: TrackX Insight Base Modular Instrument Tracker Recalled by Trackx Technology...

The Issue: The device is breaking and falling off the Nuvasive T-Handle with Hudson...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2022· Tollos

Recalled Item: Infection Control (IC) Lifting Strap used with the following Cirrus Recalled...

The Issue: Two customers reported four incidents in which the lifting strap broke while...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2022· Howmedica Osteonics Corp.

Recalled Item: Simplex HV With Gentamicin CE Recalled by Howmedica Osteonics Corp. Due to...

The Issue: Simplex HV With Gentamicin CE, 10 PACKS (P/N 6193-1-010) were distributed to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2022· Philips North America Llc

Recalled Item: Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1...

The Issue: Potential table stop due to a broken tabletop cable: On the ProxiDiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2022· Intersect ENT, Inc.

Recalled Item: Propel Mini Mometasone Furoate Sinus Implant Recalled by Intersect ENT, Inc....

The Issue: Sinus Implant product label displays incorrect product information...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Sensititre Plate Recalled by Remel Inc Due to An internal...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· CooperSurgical, Inc.

Recalled Item: NEO-fit Neonatal Endotracheal Tube Grip Recalled by CooperSurgical, Inc. Due...

The Issue: Firm has received 11 complaints involving a loose or detached metal clips,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing