Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4, E29-5553M4, E29-7270M4, E29-7272M4, E29-727A, EP4013P, EP4110N, X-2235, X29-7271M2, X-5667M8 and X-6730M5.
Reported: April 30, 2014 Initiated: March 11, 2014 #Z-1497-2014
Product Description
Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4, E29-5553M4, E29-7270M4, E29-7272M4, E29-727A, EP4013P, EP4110N, X-2235, X29-7271M2, X-5667M8 and X-6730M5.
Reason for Recall
The products are being recalled because they did not meet minimum diameter requirements.
Details
- Recalling Firm
- Teleflex Medical
- Units Affected
- 3,816 ea
- Distribution
- Worldwide Distribution - CA, CO, FL, IN, KY, MA, NM, PA, Canada, Ireland and Germany.
- Location
- Research Triangle Park, NC
Frequently Asked Questions
What product was recalled? ▼
Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4, E29-5553M4, E29-7270M4, E29-7272M4, E29-727A, EP4013P, EP4110N, X-2235, X29-7271M2, X-5667M8 and X-6730M5.. Recalled by Teleflex Medical. Units affected: 3,816 ea.
Why was this product recalled? ▼
The products are being recalled because they did not meet minimum diameter requirements.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 30, 2014. Severity: Moderate. Recall number: Z-1497-2014.
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