Reported Apr 3, 2024 · Ongoing
Baxter Supple Peri-Guard Repair Patch (new product codes): a) SPG0404, b) SPG0406, c) SPG0608, d) SPG0814, e) SPG1016
Baxter Healthcare Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
- Baxter Supple Peri-Guard
- Repair Patch (new product codes)
a) SPG0404b) SPG0406c) SPG0608d) SPG0814e) SPG1016
- Lot codes and dates
a) SPG0404UDI/DI 00085412818672b) SPG0406UDI/DI 00085412818696c) SPG0608UDI/DI 00085412818313d) SPG0814UDI/DI 00085412818375e) SPG1016UDI/DI 00085412818429ALL LOTS WITHIN EXPIRY
- Amount recalled
- 4774 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
A new contraindication was added to the IFU which states that Peri-Guard Repair Patch should not be used in neurosurgery since the product endotoxin level may be higher than the allowable limit for cerebrospinal fluid-contacting devices and Supple Peri-Guard Repair Patch should not be used in neurosurgery since the product endotoxin level may be higher than the allowable limit for cerebrospinal fluid-contacting devices.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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