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. 1,012 recalls have been distributed to North Dakota in the last 12 months.
Showing 16221–16240 of 47,938 recalls
Recalled Item: Sulfur Ointment 10% Recalled by DLC Laboratories, Inc Due to Labeling: Label...
The Issue: Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHILIPS BATTERY Recalled by Respironics California, LLC Due to Due to...
The Issue: Due to unqualified "design verification" batteries being shipped to customers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9180 Electrolyte Analyzer - Product Usage: intended to be used Recalled by...
The Issue: May display Calcium results on the screen with wrong arrow direction which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infusion Pump Recalled by Baxter Healthcare Corporation Due to Battery...
The Issue: Battery performance issues related to prolonged storage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for Recalled by Arrow...
The Issue: The lidstock / information card on the kits correctly states the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascade Abrazo aPTT Test Card - Product Usage: are to Recalled by Helena...
The Issue: Intermittent potential for shorter than expected clot times.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 6MMx 23G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX SIF 270CM 23G 4MM Recalled by Aomori Olympus Co., Ltd. Due...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAJ-247 SINGLE USE 30MM REPLACEMENT BASKET Recalled by Aomori Olympus Co.,...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SD-210U-15 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SD-240U-15 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SD-400U-15 SNAREMASTER PLUS Hot/Cold 15m Recalled by Aomori Olympus Co.,...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 3MMx 23G LOWER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 21G 6MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-201SX-4022-B ASPIRATION NEEDLE ViziShot 22G Recalled by Aomori Olympus...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KD-655U ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-401D-1321 ASPIRATION NEEDLE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 23G 6MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX SIF 270CM 23G 4MM Recalled by Aomori Olympus Co., Ltd. Due...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX SIF 270CM 23G 4MM Recalled by Aomori Olympus Co., Ltd. Due...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.