Class II

Medical Device Recall: Medline medical procedure kits labeled as follows: DENTAL, REF DYNJ909211A

MEDLINE INDUSTRIES, LP - Northfield · March 22, 2024

Reason for Recall

A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.

Distribution

Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.

States Affected

NATIONWIDE

Quantity Affected

99 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2702-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.