Pajunk Medical Systems, L.P.

FDA Regulatory Profile

Pajunk Medical Systems, L.P. appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-0278-2023, Class II) was initiated on October 10, 2022.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0278-2023Class IIPAJUNK Continuous Epidural Tray, Tuohy Epidural Needle 17G x 4" with EpiLong Soft Catheter, Closed TOctober 10, 2022