FDAClass IISeptember 18, 2024

Medline Convenience kits labeled as: 1) SH STRL recall

Medline Convenience kits labeled as: 1) SH STRL UMBILICAL ACC PACK-LF, Pack Number DYNJ0621408V; 2) SH STRL UMBILICAL ACC PACK-LF, Pack Number…

Why was Medline Convenience kits labeled as: 1) SH STRL recalled?

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

DYNJ0621408V, Lot Number 23ILB053; DYNJ0621408VH, Lot Number 23ILB053; DYNJ0864492A , Lot Number 21KMH585 ; DYNJ0864492AH, Lot Number 21KMH585 ; SAMP0545 , Lot Number 22GME387 ; SAMP0545 , Lot Number 22GME980

Product
Medline Convenience kits labeled as: 1) SH STRL UMBILICAL ACC PACK-LF, Pack Number DYNJ0621408V; 2) SH STRL UMBILICAL ACC PACK-LF, Pack Number…
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Distribution
Worldwide distribution.
Recall date
September 18, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls