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Medical Device

Medline Kits: 1) LABOR PACK-22025208-LF, Model Number: DYNJ44813D

Recall date: 2026-04-29 · Source: FDA_DEVICE
Product
Medline Kits: 1) LABOR PACK-22025208-LF, Model Number: DYNJ44813D
Reason for recall
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Units affected
1720 units
Description
Medline Kits: 1) LABOR PACK-22025208-LF, Model Number: DYNJ44813D
View official recall notice →