Atlas FDA

Aero Blue Performance Surgical Gown, XL- Sterile surgical gown Code: 41734

FDA device recall Z-0343-2023 · posted 2022-12-06 · Open, Classified

Recall details

Recalling firm
Owens & Minor Distribution, Inc.
Reason for recall
Potential open seal pouches compromising sterility resulting in the use of a non-sterile product in surgery could lead to patient infection
Action taken
Owens & Minor initiated recall by Voluntary Recall - EVENT # FCA-2022-009 letter dated 10/31/22 via email and Overnight mail. Letter states reason for recall, health risk and action to take: 1. REVIEW your inventory for the affected products. 2. SEGREGATE AND QUARANTINE all product on-hand per the Affected Product table above. 3. DESTROY or DISCARD the product per the facility s standard disposal procedure for surgical gowns. 4. COMMUNICATE this recall to staff to ensure awareness of the product issue. If the affected product identified above was further distributed, please ensure all end-users are appropriately notified of this recall notification. 5. RETURN the completed Recall Response Form and Certificate of Destruction Form to OMRA_RECALLS@owens-minor.com as soon as possible even if you have no current product inventory. If you have any questions, please email Caitlin Senter @ OMRA_RECALLS@owens-minor.com using the Event # FCA-2022-009 in the header of the response. This will ensure prompt response by the O&M Halyard, Inc, team.
Root cause
Under Investigation by firm
Status
Open, Classified
Product code
FYA
Quantity affected
72 cases (2160 pouches)
Distribution
IL, IN, WV
Date initiated
2022-10-31
Date posted
2022-12-06
Location
Mechanicsville, VA

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Related 510(k) clearances

RecordFirmDate
Aero Blue Performance Surgical Gowns (K192362)O&M Halyard, Inc.2019-12-13