Complete FDA and NHTSA recall records dated in July 2024.
These records include useful source details for the selected month.
GE HealthCare has become aware of the potential for loss of monitoring on CARESCAPE Canvas 1000, CARESCAPE Canvas Smart Display, and certain versions of CARESCAPE B850 and CARESCAPE B650…
GE HealthCare has become aware of the potential for loss of monitoring on CARESCAPE Canvas 1000, CARESCAPE Canvas Smart Display, and certain versions of CARESCAPE B850 and CARESCAPE B650…
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Due to a component change, the console part of a circulatory support system may not conform to the IEC 61000-4-5 standard, so if subjected to a power surge above 1.8kV and up to 2.0 kV, the…
Potential for there to be a fluid ingress into the handle of the harvesting tool, which may lead to the device not providing cautery or providing cautery when not intended.
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
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
