Class II

Medical Device Recall: MEDLINE M1S0179 STRL TAPE/PEN PACK, Product Code P519582A

MEDLINE INDUSTRIES, LP - Northfield · February 23, 2024

Reason for Recall

Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.

Distribution

Worldwide distribution - US Nationwide and the countries of Panama, Canada.

States Affected

NATIONWIDE

Quantity Affected

4200 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1452-2024

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.