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. 1,061 recalls have been distributed to North Dakota in the last 12 months.
Showing 10281–10300 of 27,512 recalls
Recalled Item: NEEDLEMASTER 6MMx 25G UPPER 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 25G 4MM 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: NEEDLEMASTER 3MMx 26G 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 23G 5MM 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 LOWER 25G 6MM 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: NEEDLEMASTER 1.8MMx 26G 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: PBD-203-0710 BILIARY STENT 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-25 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-200H-8022 22G EZSHOT ASPIRATION NEEDLE 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: K-204 GUIDE SHEATH KIT 2.6MM 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: B5-2Q BALLOON CATHETER 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: K-202 GUIDE SHEATH Kit 2.0MM 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: B7-2Q BALLOON CATHETER 13MM DIA 3.2 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 UP 2.8MMCH 25G 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: KD-650L 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: PBD-203-0704 BILIARY STENT 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: ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG - Product Recalled by Beckman...
The Issue: The Quality Control (QC) card has a label error for the standard deviation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tourni-Cot - Universal Recalled by Mar-Med Co Due to A failure can occur if...
The Issue: A failure can occur if the user attempts to remove the device by partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm...
The Issue: Potential for the battery to lose its ability to be recharged.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ Diagnostic Ultrasound System Recalled by Philips Ultrasound Inc...
The Issue: Control panel arm assembly could have missing or loose screws where undue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.