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. 2,375 recalls have been distributed to North Dakota in the last 12 months.
Showing 23101–23120 of 27,512 recalls
Recalled Item: Tapered-Screw Vent Implant Recalled by Zimmer, Inc. Due to Zimmer Dental is...
The Issue: Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx Only...
The Issue: Genesis BPS is recalling numerous devices since they did not notify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Immunodiagnostic Products CA 19-9 Calibrators and Reagent Packs...
The Issue: Customers may receive positively biased results when using VITROS¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...
The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiomat M+ NIF 14 x 17 Recalled by AGFA Healthcare Corp. Due to Some sheets...
The Issue: Some sheets of the medical screen film are fogged.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use for the blue endo MOREsolution Electromechanical...
The Issue: Some pages of the Instructions for Use were omitted, including pages...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension EXL Integrated Chemistry System in vitro diagnostic...
The Issue: The Reagent Lid hinge may lose its effectiveness and slowly shift downward...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a Recalled...
The Issue: The cautery that is provided with the Gelweave graft in the box has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Chemistry Wash (RD701) is an accessory of the Recalled by...
The Issue: Siemens Healthcare Diagnostics has received complaints for the Dimension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***Baxter***Non-DEHP***BURETROL Solution Set 105" (2.7 m) Recalled by Baxter...
The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***Baxter***BURETROL Solution Set***105" (2.7 m) 150 mL Burette***Drip...
The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip...
The Issue: Baxter Healthcare Corporation is voluntarily issuing a recall for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS Tibial Insert Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Post-Op Surgical Kits . Kit includes: Amerigel Wound Dressing...
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management....
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patella 38mm Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pivot Bipolar Cup 22x42/43-51/53mm Recalled by Ortho Development Corporation...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibila Insert CK Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Hydrogel Saturated Gauze Dressing Recalled by Amerx Health Care...
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Daily Dressing Advanced 3-in-1 Hydrogel Recalled by Amerx Health...
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.