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. 2,363 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,363 in last 12 months

Showing 2674126760 of 27,512 recalls

Medical DeviceJuly 2, 2012· Mc-NEIL-PPC, Inc.

Recalled Item: KY LIQUIBEADS Vaginal Moisturizer Recalled by Mc-NEIL-PPC, Inc. Due to...

The Issue: Johnson & Johnson Healthcare Products (JJHP) is voluntarily recalling this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Philips Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due...

The Issue: Philips Healthcare was notified that several of the sixteen bolts securing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2012· Varian Medical Systems, Inc. Oncology Systems

Recalled Item: Varian brand Varian ARIA Oncology Information System Recalled by Varian...

The Issue: A software anomaly has been identified with the Import Export Application...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2012· Draeger Medical Systems, Inc.

Recalled Item: Drager PT 4000 Phototherapy System Recalled by Draeger Medical Systems, Inc....

The Issue: A routine internal quality check found that the Drager PT 4000 Phototherapy...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2012· Beekley Corporation

Recalled Item: Bella Blanket Protective Coverlet Recalled by Beekley Corporation Due to...

The Issue: Imaging artifact can occur on mammogram result

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2012· Ethicon, Inc.

Recalled Item: EVICEL Fibrin Sealant (Human) Rx Only. Manufacturer: Omrix...

The Issue: Ethicon and Omrix Biopharmaceuticals have received reports of air or gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2012· Merge Healthcare, Inc.

Recalled Item: Merge HEMO software. Recalled by Merge Healthcare, Inc. Due to The...

The Issue: The International Normalized Ratio (INR) value displayed in the study report...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module model 8100. Subsequent product code: FPA The Recalled by...

The Issue: The recall was initiated because Carefusion identified a potential risk...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 29, 2012· BD Biosciences, Systems & Reagents

Recalled Item: BD FACS 7-color Setup beads BD Biosciences Recalled by BD Biosciences,...

The Issue: Incorrect version of the CD was included with BD FACS 7 Color Setup Beads.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Chorus Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Encore Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Sara Plus Mobile Patient Lifter Recalled by Arjo, Inc. dba ArjoHuntleigh Due...

The Issue: ArjoHuntleigh has received a limited number of customer reports concerning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2012· C.R. Bard, Inc., Urological Division

Recalled Item: Bard Foley procedural trays packaged in breather bags. The product Recalled...

The Issue: Incomplete seal on sterile packages of product.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2012· Advanced Sterilization Products

Recalled Item: STERRAD Cyclesure Biological Indicator (BI) Recalled by Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling certain lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DGXN Slides --- [REF] 834 3386. Product Recalled...

The Issue: Ortho Clinical Diagnostics revised the VITROS Chemistry Products DGXN Slides...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Mar Cor Purification

Recalled Item: Mar Cor Purification CWP Reverse Osmosis System. Models 101 Recalled by Mar...

The Issue: There exists a potential situation with the crimp connection at the pump...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· KCI USA, Inc.

Recalled Item: RotoRest Delta Kinetic Therapy System INDICATIONS: Treatment and prevention...

The Issue: The firm is initiating a voluntary medical device correction for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair. The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair. The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing