Recall Atlas
Drugs & medicalClass II

GRI Medical & Electronic Technology Co., Ltd. recalls HALYARD Laparoscopy Comprehensive Pack II REF: 49332

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

Read the official notice →
Date
2026-10-14
Country
United States
Brand
GRI Medical & Electronic Technology Co., Ltd.
Product
HALYARD Laparoscopy Comprehensive Pack II REF: 49332
Classification
Class II
Units
US Nationwide distribution in the state of MS.
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

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  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

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