Reported Sep 9, 2015 · Terminated
Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129 Product Usage: Sterile Delivery are indicated for…
Covidien LLC
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: Covidien LLC · 60 Middletown Ave · North Haven, CT · 06473-3908
Is this the product you have?
- Monoject 0.9% Saline
- Flush Prefill Double Pouch Item Code8881570129
- Product UsageSterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access devices
- Lot codes and dates
- Lot Numbers
P15035P15036P15037P15041P15042P15046P15047P15048P15049P15056P15057P15058P15059P15063P15064P15069P15070P15071P15078P15079P15080P15081P15091
- Lot Numbers
- Amount recalled
- 207,876
This recall covers 16 products
The agency filed one notice per product. You are reading one of them; the other 15 are below.
3 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Sterility may be compromised
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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