VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal pelvic organ prolapse and for use in the repair of rectal prolapse excluding rectocele.
Reported: January 20, 2021 Initiated: December 11, 2020 #Z-0807-2021
Product Description
VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal pelvic organ prolapse and for use in the repair of rectal prolapse excluding rectocele.
Reason for Recall
VERITAS Collagen Matrix 12x25 cm Patches may have undersized width dimensions.
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 192 units
- Distribution
- Worldwide distribution - US Nationwide distribution including in the states of FL, IL, MA, MS, OH, OR, TX, VA, WA, WV and the countries of Australia, Poland, and United Kingdom.
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal pelvic organ prolapse and for use in the repair of rectal prolapse excluding rectocele.. Recalled by Baxter Healthcare Corporation. Units affected: 192 units.
Why was this product recalled? ▼
VERITAS Collagen Matrix 12x25 cm Patches may have undersized width dimensions.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 20, 2021. Severity: Moderate. Recall number: Z-0807-2021.
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