a — Class III medical device recall Z-1806-2022

Ongoing recall by Mckesson Medical-Surgical Inc. Corporate Office, reported 2022-10-05, distributed nationwide. Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperature

Recall number	`Z-1806-2022`
Product type	Medical device
Classification	Class III
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	Mckesson Medical-Surgical Inc. Corporate Office, Richmond, VA, United States
Recall initiated	2022-05-25
Classified	2022-09-26
Reported by FDA	2022-10-05
Distributed	Nationwide (US)
Reason classes	temperature control
UPC / GTIN / UDI-DI	`00612479243545`, `00612479253018`, `00612479253025`, `00612479253032`, `00612479253049`, `00612479253056`, `00612479253063`
Model numbers	`177200`, `177400`, `87400`

Product

a. ADVANCED MEDICAL SOLUTIONS McKesson DRESSING, WOUND GELLING FIBERHIGH-ABSRB 4"X4 3/4" (10/BX) Catalog #87400. b. ADVANCED MEDICAL SOLUTIONS McKesson DRESSING, WND GELLING FIBER HIABSRB AG 4X4.75 (10/BX 10BX/CS Catalog #177400. c. ADVANCED MEDICAL SOLUTIONS McKesson DRESSING, WOUND GELLING FIBERHI-ABSRB AG 2X2 (10/BX 10BX/CS Catalog # 177200

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. This device with this specific storage temperature deviation is not likely to cause adverse health consequences.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1806-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.