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. 2,503 recalls have been distributed to North Dakota in the last 12 months.
Showing 12641–12660 of 27,512 recalls
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm Recalled by...
The Issue: One lot of 3.5 mm twist drills were incorrectly laser etched as 2.5 mm the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475...
The Issue: During shipping, it is possible for the Aequalis Ascend Flex humeral stem to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...
The Issue: The rotary therapy selector switch may fail, resulting in unexpected device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levo Arm Label: LEVO ARM MIZUHO OSI Recalled by Mizuho OSI Due to Due to the...
The Issue: Due to the potential for fluid ingress into the Arm which could affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urine Electrolyte Diluent Recalled by Ortho Clinical Diagnostics Inc Due to...
The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7% BSA (Bovine Serum Albumin) Recalled by Ortho Clinical Diagnostics Inc Due...
The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiofrequency Grounding Pad Recalled by Abbott Medical Due to Affected lots...
The Issue: Affected lots were manufactured with the protective release liner in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575...
The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547...
The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...
The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...
The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare Ceiling Mounted Surgical Light System Recalled by...
The Issue: The firm has become aware that there is a likelihood that a missing snap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Through a customer complaint and and internal investigation it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroTek Temporal Sensor Cable Gold - Long Length Recalled by LIFELINES...
The Issue: Potential for one of the four temporal electrode cables used in with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroTek Temporal Sensor Cable Gold - Long Length Recalled by LIFELINES...
The Issue: Potential for one of the four temporal electrode cables used in with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5mm Aresenal Screw Drill Bit Recalled by Trilliant Surgical, LLC Due to...
The Issue: Labeling Error; specifically, drill bits from lots # TSL008495A are marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.