FDA Device Recalls

Recalls /

#206459

Product

MEDLINE SWABSTICKS PVP 3 PK, Product Code DYNDA2724

FDA product code
OJUSkin Prep Tray
Device class
Class 1
Medical specialty
General, Plastic Surgery
Affected lot / code info
UDI/DI 20193489190790 (case) 10193489190793 (each), Lot Numbers: 2023071290, 2023091890

Why it was recalled

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.

Root cause (FDA determination)

Process control

Action the firm took

Medline Industries, LP, issued a Medical Device Recall notice to its consignees on 02/27/2024 via email and USPS First Class mail. The notice explained the problem with the devices, risk, and requested that the products be destroyed at the consignee. Distributors were directed to notify their customers.

Recalling firm

Firm
MEDLINE INDUSTRIES, LP Northfield
Address
3 Lakes Dr, Northfield, Illinois 60093-2753

Distribution

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

Timeline

Recall initiated
2024-02-23
Posted by FDA
2024-03-29
Status

Source: openFDA Device Recall endpoint. Recall record ID #206459. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

— recall: MEDLINE SWABSTICKS PVP 3 PK, Product Code DYNDA2724 · FDA Device Recalls