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PILLING
TELEFLEX INCORPORATED · Model IPN007750 · UDI-DI 24026704530407
GDM
Prescription
10
510(k) clearances
56
Adverse events (3 deaths)
4
Recalls
113
Facilities
Description
ADAPTER VENTURI NEEDLE-SANDERS
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-06-27 | Spiggle & Theis Mt Gmbh | Affected product show elevated cytotoxicity values. Use of affected injection needles may present a risk of intolerance reaction or allergic reaction. |
| 2015-01-08 | Teleflex Medical | Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 14087 |
| 2009-09-01 | Medical Device Technologies, Inc. | Medical Device Technologies doing business as Angiotech has conducted a recall on Angiotech Breast Localization Needles, Soft Tissue Biopsy Needles, Vascular Access Needles, Bone B |
| 2009-04-06 | Remington Medical Inc. | Incorrect needle (Franseen Needle, FNM-1806) was packaged as a Chiba Needle Marked. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.