Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

SHPI LIftLoc Safety Infusion Sets

FDA Recall Z-0837-03 · Posted 2003-05-15

Recalling FirmSpecialized Health Products, Inc.
Recall StatusTerminated
Product CodeFPA
Date Initiated2003-04-17
Date Terminated2003-08-20
Product Quantity2240 units

Reason for Recall

Pouch seals on Safety Infusion Sets may be defective, possibly compromising sterility.

Firm Action

The single consignee (BAS) was notified by lettter on 4/14/03.

Root Cause

Other

Distribution Pattern

Utah.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K013394LIFTLOC SAFETY INFUSION SETSpecialized Health Products, Inc. · 2001-11-08

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑