Cardinal Health ROYALSILK LARGE, Gown. Item Code 9518 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ROYALSILK LARGE, Gown. Item Code 9518
Brand
Cardinal Health
Lot Codes / Batch Numbers
244 or greater is affected OR " " If made in 2019, any value is affected
Products Sold
Lot Numbers: XXXXJXXX Single-Sterile Lot Format: YYMRJXXX Where: YY Last two digits of the year ( 18 or '19) M Month in alpha code " If made in 2018 o J for September o K for October o L for November OR o M for December " If made in 2019, any value is affected R Product revision or suffix P Facility code is letter J XXX Sequential Number - Monthly reset OR Bulk Non-Sterile Lot Format: XXXYRPQ Where: XXX Elapsed days of year " " If made in 2018, 244 or greater is affected OR " " If made in 2019, any value is affected; see below for year made identifier Y Last character of year gown was made (2018 or 2019) R Product Revision P Facility code is letter J Q Plant shift identifier; this identifier was added during the affected time period and therefore older product may not contain this digit in the lot number
Cardinal Health is recalling ROYALSILK LARGE, Gown. Item Code 9518 due to The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
Recommended Action
Per FDA guidance
A letter dated 1/11/20 informed customers that: Cardinal Health has become aware of a quality issue related to the manufacture of certain AAMI Level 3 surgical gowns. We have initiated an investigation, placed a hold on product inventory, and are working with the U.S. Food and Drug Administration (FDA) to address this issue. This inventory hold affects certain lots of bulk non-sterile and single-sterile Cardinal Health" surgical gowns and Presource procedure packs that include these surgical gowns. Your local sales representative will provide specific details. Cardinal Health intends to initiate a product recall and will provide you with instructions soon. In the meantime, discontinue use and segregate all affected surgical gowns and Presource procedural packs that include these affected surgical gowns from your current inventory. These actions will cause a supply disruption, and we are prepared to suggest alternate surgical gowns and pack components you may need during this time. Please note that our process will initially place all impacted Presource procedure packs on a short-term hold as we work through the process. This should not impact your broader base of inventory. For Presource packs currently in production, we will include gowns with similar fit, form and function, where possible, with no change in cost, or run without the product or suggest an alternate, comparable single-sterile gown. Your sales representative will work with you to identify alternative pack components needed to perform your procedures. We recognize the criticality of our gowns and procedure packs to performing surgeries, and we apologize for the challenges this supply disruption will cause. Cardinal Health puts the safety of patients and health care workers first. We appreciate your understanding and patience during this time. An Urgent Medical Device Recall notification letter dated 1/21/20 was sent to customers. Actions Required: 1. CHECK all storage and usage
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026