FDA recall Z-1802-2022

Mckesson Medical-Surgical Inc. Corporate Office · Class III · device

Product

Medical Monofilament Manufacturing MONOFILIMENT TEST, SENSORY F/FOOT 10GM (40/PK) Model Number: AM140

Reason for recall

Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Distribution

US Nationwide distribution.

Key facts

Status: Ongoing
Initiation date: 2022-05-25
Report date: 2022-10-05
Voluntary/Mandated: Voluntary: Firm initiated
Location: Richmond, VA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1802-2022