Wolf, Henke Sass, Gmbh Henke-Ject-2 part luer sterile single use syringes - used for recall — FDA Z-2642-2023
Sterile barrier might be damaged compromising the sterility of the device.
Overview of recall records associated with Wolf, Henke Sass, Gmbh, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Sterile barrier might be damaged compromising the sterility of the device.
This page summarizes recall records in which the official source identifies Wolf, Henke Sass, Gmbh as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.