Medical Device Recall: Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes EXTREMITY PACK DYNJ34846C HAND PACK DYNJ83218A, DYNJ85396 LAMINECTOMY DYNJ905156R MAJOR EXTREMITY
Medline Industries, LP · February 27, 2026
Reason for Recall
Unapproved design changes to the products outside of the 510(k) clearance.
Product Description
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes EXTREMITY PACK DYNJ34846C HAND PACK DYNJ83218A, DYNJ85396 LAMINECTOMY DYNJ905156R MAJOR EXTREMITY DYNJ905159L, DYNJ905159M MAJOR EXTREMITY PACK DYNJ69926A PODIATRY PACK DYNJ41250B
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.
States Affected
NATIONWIDE
Quantity Affected
270,311 total
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1887-2026
Status: ongoing
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