Reported Apr 30, 2014 · Terminated
Monofilament and Multifilament Non-absorbable Steel Suture; Product Codes: 0520197-2, 29-727, 29-7270M4, 29-7281M4,…
Teleflex Medical
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: Teleflex Medical · 2917 Weck Dr. · Research Triangle Park, NC · 27709
Is this the product you have?
- Monofilament and Multifilament Non-absorbable Steel Suture
- Product Codes
0520197-229-72729-7270M429-7281M4E29-5553M4E29-7270M4E29-7272M4E29-727AEP4013PEP4110NX-2235X29-7271M2X-5667M8 and X-6730M5
- Lot codes and dates
13 of 13 products
Products covered by this recall Model / number Product as published 0520197-2Lot number: 02H1001071 29-727Lot numbers: 02M1101954, 02C1201003, and 02C1201646 29-7270M4Lot number: 02D1100604 29-7281M4Lot number: 02M1002679 E29-5553M4Lot number: 02B1300245 E29-7270M4Lot number: 02J1001576 E29-7272M4Lot number: 02D1003015 E29-727ALot number: 02F1101062 EP4013PLot number: 02L0800898 EP4110NLot number: 02H0900483 X-2235Lot numbers: 02E1102068, 02F1101041, 02F1201500, and 02G1201230 X29-7271M2Lot number: 02K1100784 X-6730M5Product Code: X-5667M8 and , Lot number: 02G1300492. - Amount recalled
- 3,816 ea
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
The products are being recalled because they did not meet minimum diameter requirements.
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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