Reported May 15, 2013 · Terminated
A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set, 5.7", Vol. 0.8 mL, 2 Injection Sites, Male Luer Lock…
Baxter Healthcare Corp.
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 Corp. · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
- A) Product Code 2N3371
Non-DEHP Y-Type Catheter Extension Set5.7"Vol. 0.8 mL2 Injection SitesMale Luer Lock Adapter
- Single use only Product UsageThis device is indicated for use in blood sampling and the administration of solutions. The InterLink Injection Site feature is intended to eliminate accidental needle sticks when used in conjunction with an InterLink Cannula as part of an I.V. needless access system
- Lot codes and dates
- A) Product Code 2N3371
Lots R12H23076R12H30097R12I0707R12I08059R12I25046R12I2607R12J11052R12J12068R12J13058R12K17057R12L10084R13A12057
- A) Product Code 2N3371
- Amount recalled
- A) Product Code 2N3371: 228,200 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
- Nationwide
- PR
Why it was recalled
Customers have reported that when separating an individual package from its attached grouping, the adjacent package has opened, compromising its sterile barrier properties.
This product could cause temporary or reversible health problems — stop using it.
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