Wolf, Henke Sass, Gmbh

FDA Regulatory Profile

Wolf, Henke Sass, 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-2642-2023, Class II) was initiated on July 27, 2023.

Summary

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

Recent Recalls

NumberClassProductDate
Z-2642-2023Class IIHenke-Ject-2 part luer sterile single use syringes - used for intravenous, intramuscular, subcutaneoJuly 27, 2023