Spiggle & Theis Mt Gmbh

FDA Regulatory Profile

Spiggle & Theis Mt Gmbh appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2331-2025, Class II) was initiated on June 27, 2025.

Summary

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

Recent Recalls

NumberClassProductDate
Z-2331-2025Class IIInjection needle, bayonet, Luer-Lock, 1. Model no. 50-353-23, working length 25 cm, total length June 27, 2025