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Field reports on stuff that let you down

FDA device recallMedications· GRI Medical & Electronic Technology Co., Ltd.

HALYARD Laparoscopy Comprehensive Pack II REF: 49332

Official notice from a government agency or its published feed.

HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Reason: Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter
Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · US Nationwide distribution in the state of MS.

Hazard: Laparoscopy packs labeled as "latex free" were found to contain a latex urethral catheter

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