Spiggle & Theis Mt Gmbh Injection needle, bayonet, Luer-Lock, 1 recall — FDA Z-2331-2025
Affected product show elevated cytotoxicity values. Use of affected injection needles may present a risk of intolerance reaction or allergic reaction.
Overview of recall records associated with Spiggle & Theis Mt Gmbh, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Affected product show elevated cytotoxicity values. Use of affected injection needles may present a risk of intolerance reaction or allergic reaction.
This page summarizes recall records in which the official source identifies Spiggle & Theis Mt 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.