Device recall: SmartGown Breathable Surgical Gowns with raglan sleeves X-large, X-long, A-line SKU: 32474
Class II FDA enforcement event 89015. Recall start date: . Status in the FDA record: Ongoing.
Reason for recall, in the words of FDA
Potential for open packaging seals compromising the sterility of the surgical gowns
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Cardinal Health started this device recall on 2 Nov 2021. The firm address in the FDA record is in Waukegan, IL. FDA put the recall in Class II. FDA event 89015 has 11 product records. The first FDA enforcement report date is 22 Dec 2021. The record gives the status Ongoing.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Worldwide distribution - US Nationwide and the countries of Chile, Thailand, Canada, Israel, LATAM Dist.Qatar, LATAM/Panama, LATAM/Mexico, LATAM/Colombia, LATAM/Costa Rica.
Recalling firm
Cardinal Health, Waukegan, IL.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
11 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-0368-2022 | SmartGown Breathable Surgical Gowns with raglan sleeves X-large, X-long, A-line SKU: 32474 | 224,312 units | Class II | Ongoing | 22 Dec 2021 |
| Z-0369-2022 | SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns-Large SKU: 9011 | 169,262 units | Class II | Ongoing | 22 Dec 2021 |
| Z-0370-2022 | SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns-X-Large SKU: 9041 | 231,219 units | Class II | Ongoing | 22 Dec 2021 |
| Z-0371-2022 | SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns X-large, X-long SKU: 9041EL | 363,480 units | Class II | Ongoing | 22 Dec 2021 |
| Z-0372-2022 | Cardinal Health Poly-Reinforced Surgical Gowns Large SKU: 9010 | 17,174 units | Class II | Ongoing | 22 Dec 2021 |
| Z-0373-2022 | Cardinal Health Poly-Reinforced Surgical Gowns X-large SKU: 9040 | 146,939 units | Class II | Ongoing | 22 Dec 2021 |
| Z-0374-2022 | Cardinal Health Poly-Reinforced Surgical Gowns XX-large SKU: 9070 | 29,893 units | Class II | Ongoing | 22 Dec 2021 |
| Z-0375-2022 | RoyalSilk Non-Reinforced Surgical Gowns Large SKU: 9518 | 364,481 units | Class II | Ongoing | 22 Dec 2021 |
| Z-0376-2022 | RoyalSilk Non-Reinforced Surgical Gowns X-large SKU: 9548 | 270,839 units | Class II | Ongoing | 22 Dec 2021 |
| Z-0377-2022 | RoyalSilk Non-Reinforced Surgical Gowns XX-large SKU: 9578 | 9,990 units | Class II | Ongoing | 22 Dec 2021 |
| Z-0378-2022 | RoyalSilk Non-Reinforced Surgical Gowns XXX-large, X-long SKU: 95998 | 8,950 units | Class II | Ongoing | 22 Dec 2021 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2021
- 900
- Share of these events in Class II
- 89%
- Product records in this event
- 11Median of the firm: 1
- Events of the firm on the register
- 12
Other events of the firm
Official channels
- FDA enforcement report Z-0368-2022The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 89015. https://recallregister.com/fda/ii/89015/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Worldwide distribution - US Nationwide and the countries of Chile, Thailand, Canada, Israel, LATAM Dist.Qatar, LATAM/Panama, LATAM/Mexico, LATAM/Colombia, LATAM/Costa Rica.
- What quantity of product is in FDA event 89015?
- The event has 11 product records. The first record gives this quantity:
224,312 units
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2021 have the same class?
- 89% of the 900 device events that started in 2021 are in Class II.