Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1362-2019 — Technopath Multichem S Plus Level 1 - Product Usage: Multichem S Plus (Assayed) is intended for use as an assayed quality control serum to monitor the precision of laboratory testing procedures for the analytes listed in the package insert.

U.S. FDA — Device Enforcement · United States · 2019-04-09 · Class III

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1362-2019
Date of alert
2019-04-09
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Abbott Laboratories
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
18004181
Reported risk: Devices were delivered without the required dry ice.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.