Nihon Kohden Adult Cap-ONE Biteblock REF YG-227T The cap-ONE Biteblock is intended to sample recall — FDA Z-0314-2025
Due to products being shipped/distributed to customers after the products expiration date had past.
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.
Due to products being shipped/distributed to customers after the products expiration date had past.
A Gen 5 tail piece was assembled to a Gen 4 Finished Device, resulting in a 0.178" difference in the end of the endoscope slot to the end of the tail piece. This allows the scope to move…
There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS))…
DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil…
Product defect where the X-ray detectable barium strip (aka radio-opaque marker) becomes detached from the sponge (pattie). May delay surgical process as the surgeon may require extra time…
The Bipolar assembly contains an oversized Retainer Ring.
There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS))…
DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil…
There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS))…
Undeclared allergen: milk
Acidified product is recalled due to lack production record.
Acidified product is recalled due to lack production record.
Acidified Chai Tea product is recalled due to lack production record.
Acidified product is recalled due to lack production record.
Undeclared sesame
Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.
Acidified product is recalled due to lack production record.
Acidified product is recalled due to lack production record.
Acidified Chai Tea product is recalled due to lack production record.
Undeclared sesame
Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.
Undeclared allergens; wheat, soy, and eggs.
Acidified Chai Tea product is recalled due to lack production record.
Acidified product is recalled due to lack production record.
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.