Covidien LLC: Medical Device Recall in 2015 - (Recall #: Z-2525-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: August 6, 2015

Date Posted: September 9, 2015

Recall Number: Z-2525-2015

Event ID: 71893

Reason for Recall:

Sterility may be compromised

Status: Terminated

Product Quantity: 207,876

Code Information:

Lot Numbers: P15035 P15036 P15037 P15041 P15042 P15046 P15047 P15048 P15049 P15056 P15057 P15058 P15059 P15063 P15064 P15069 P15070 P15071 P15078 P15079 P15080 P15081 P15091

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated