Recall Z-1226-2023— Preat Corp

Class III · Ongoing

Class III FDA medical device recall by Preat Corp, initiated 2023-02-01. FDA's recall record names no specific 510(k) clearance for this event. Product: PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.. Reason: Product is labeled with an incorrect expiration date..

Recalling firm
Preat Corp
Classification
Class III
Status
Ongoing
Initiated
2023-02-01
Firm location
Santa Maria, CA, United States

Product description

PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.

Reason for recall

Product is labeled with an incorrect expiration date.

Data sourced from openFDA. This site is unofficial and independent of the FDA.