Medtronic COBALT XT VR MRI SureScan, Model Number DVPA2D1, Implantable Cardioverter recall — FDA Z-2210-2024
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Complete FDA and NHTSA recall records dated in 2024, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Due to inadvertently disconnecting grounding cable of ultrasound system could result in electrical shock, electrical interference and/or equipment malfunction.
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Undeclared wheat and milk (foreign language labeling)
Possibly contaminated with Listeria monocytogenes
Product contains Yellow Oleander
Possibly contaminated with Listeria monocytogenes
Plastic material. The piece of plastic material was detected in a 40lb. cheese block and smaller fragments of the plastic material may be found in the cheese slices.
Product has incorrect back label that does not declare pecans are present in the product.
FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.
Possibly contaminated with Listeria monocytogenes
Undeclared wheat and milk (foreign language labeling)
Undeclared allergen - coconut
Product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.
Salmonella contamination
Sub-potent Drug
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the proposed interim limit.
Lack of Assurance of Sterility-The potential for incomplete crimp seals.
Lack of Assurance of Sterility-The potential for incomplete crimp seals.
Failed Dissolution Specifications - did not meet the acceptance criteria for IVR Level 3 testing at 9 months 2-8¿C followed by 6 weeks at 25¿C
Honda (America Honda Motor Co.) is recalling certain 2024 CR-V vehicles. The tire identification number (TIN) is missing the four-digit date code. As such, these vehicles fail to comply…
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.