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. 2,529 recalls have been distributed to North Dakota in the last 12 months.
Showing 10581–10600 of 27,512 recalls
Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Westmed DISPOSABLE RESPIRATORY PRODUCTS NON-REBREATHER MASK Recalled by...
The Issue: There is a potential that the fitment between the oxygen delivery tube and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Capiox FX25 (West) Advance Oxygenator- with left port Recalled by Terumo...
The Issue: Capiox FX25 Advance oxygenator may be the incorrect configuration (East vs....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4 Recalled by RAYSEARCH LABORATORIES AB Due to Two issues were...
The Issue: Two issues were found with the treatment plan report: 1) There may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instruction Manual for Mayfield A2000 Skull Cap - Product Usage: Recalled by...
The Issue: Revised Instruction Manual to the most accurate illustration for Mayfield...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI 380 Electrocardiograph - Product Usage: intended to be a...
The Issue: The radio within the device can become disassociated with the wireless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap Extended Life PD Transfer Set Recalled by Baxter Healthcare...
The Issue: Potential for no-flow and leaks under the twist clamp.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved...
The Issue: On November 10, 2020, it was discovered that there are post- processing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter Recalled by Applied...
The Issue: The products subject to this recall may contain obvious, incorrect pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoPatch SG Pulmonary Human Cardiac Patch. The patch is cryopreserved...
The Issue: On November 10, 2020, it was discovered that there are post- processing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROKERA Plus Recalled by TissueTech, Inc. Due to Potential exposure of...
The Issue: Potential exposure of product to microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROKERA Recalled by TissueTech, Inc. Due to Potential exposure of product to...
The Issue: Potential exposure of product to microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROKERA Slim Recalled by TissueTech, Inc. Due to Potential exposure of...
The Issue: Potential exposure of product to microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended...
The Issue: Due to a potential software issue, the display may show the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-ACT Actalyke Clotting Test Tubes that are used in the: Recalled by Helena...
The Issue: Due to complaints received associated with cracked/split test tube caps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Mobile X-Ray System Recalled by Shimadzu Medical Systems Due to...
The Issue: There is a potential that the adjustable handle option on the X-Ray system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Aquilion Prime SP Recalled by Canon Medical System, USA, INC. Due to A...
The Issue: A software problem has been identified which could result in the CT Scanner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte Liquid Acid concentrate drums Recalled by Fresenius Medical Care...
The Issue: The sodium and/or calcium levels in these concentrates were below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...
The Issue: The sodium and/or calcium levels in these concentrates were below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte Liquid Acid concentrate drums Recalled by Fresenius Medical Care...
The Issue: The sodium and/or calcium levels in these concentrates were below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.