FDA Device Intelligence
HomeMEDLINE INDUSTRIES, INC. › ABS Med Distraction Pin

ABS Med Distraction Pin

MEDLINE INDUSTRIES, INC. · Model MDS9091212 · UDI-DI 00818614022635

LYQ Prescription
3
510(k) clearances
9
Adverse events
2
Recalls
22
Facilities

Description

ABS Med Distraction Pin , 12MM Pouch

Recalls

DateFirmReason
2017-05-10Zimmer Biomet Spine Inc.Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs because when applying torque to tighten the closur
2015-01-13Medtronic Sofamor Danek USA IncThe product, labeled as containing, one bevel-tipped instrument and one diamond-tipped instrument, may contain either two bevel-tipped instruments or two diamond-tipped instruments

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data 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.