Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access devices.
Reported: September 9, 2015 Initiated: August 6, 2015 #Z-2525-2015
Product Description
Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access devices.
Reason for Recall
Sterility may be compromised
Details
- Recalling Firm
- Covidien LLC
- Units Affected
- 207,876
- Distribution
- US Nationwide Distribution
- Location
- North Haven, CT
Frequently Asked Questions
What product was recalled? ▼
Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access devices.. Recalled by Covidien LLC. Units affected: 207,876.
Why was this product recalled? ▼
Sterility may be compromised
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 9, 2015. Severity: Moderate. Recall number: Z-2525-2015.
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