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

Recall Z-2153-2014 — Panthera-Puncher 9 . Panthera-Puncher 9 is a sample transfer instrument for professional use. The sample, a dried blood disk, is extracted from a larger area of the sample (dried blood spot) by punching the disk of the specified size to a sample collection vessel, e.g. a 96-well microtiter plat

U.S. FDA — Device Enforcement · United States · 2014-07-01 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2153-2014
Date of alert: 2014-07-01
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: PerkinElmer Health Sciences, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 20810001

Reported risk: Risk of incorrect results from samples prepared with Panthera-Puncher 9

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.

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