FDA-Device2026-02-18Class IIPACKAGING DEFECT
Medline suture removal kit recalled for open BD ChloraPrep swab packaging
Nationwide distributionMedical devices
What this means
Medline is recalling specific lots of suture removal kits that contain BD ChloraPrep Triple Swabsticks with potentially open or compromised packaging seals. An open seal on the applicators could allow contamination of the sterile product before use. No injuries have been reported.
- Check if you have Medline suture removal kit SKU DYNDR1277A, Lot 25EBO576
- Stop using the kit immediately if you have this lot number
- Contact Medline or your supplier for instructions on replacement or disposal
- Do not use the swabsticks if the applicator packaging appears open or damaged
The agency's original wording
Hazard
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide distribution.
Affected count
2448 kits
Manufactured in
3 Lakes Dr, N/A, Northfield, IL, United States
Products
Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY, Kit SKU DYNDR1277A
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1332-2026More Medline recalls
- FDA-Device2026-09-09Medline Convenience Kits recalled for potential sterility breach in antiseptic applicators
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for contamination risk
- FDA-Device2026-09-09Medline Convenience Kits recalled for sterility packaging breach risk
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for defective packaging seals
- FDA-Device2026-09-09Medline Arterial Line Insertion Kit recalled for sterility packaging breach risk
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