Recalls / —
—#85871
Product
Merit Medical Sysems, Inc. Pressure Infusor Bag MERITMEDICAL 500 ml Pressure Infusor Bag CATALOG NUMBER PIB500 Used to apply pressure to a sealed bag of sterile fluid.
- FDA product code
- KZD — Infusor, Pressure, For I.V. Bags
- Device class
- Class 1
- Medical specialty
- General Hospital
- Affected lot / code info
- Lot #9H42824
Why it was recalled
Potential sterility breach caused by excessive shipment damage.
Root cause (FDA determination)
Other
Action the firm took
Merit Medical Customers were contacted directly by phone and letter on 9/29/09. Customers were instructed to identify and quarantine all unused affected product. Further information was available at 801-208-4365.
Recalling firm
- Firm
- Merit Medical Systems, Inc.
- Address
- 1600 Merit Pkwy South, Jordan, Utah 84095
Distribution
- Distribution pattern
- US (AL, LA, MO, KY, TN, GA). No military, government or foreign distribution.
Timeline
- Recall initiated
- 2009-09-29
- Posted by FDA
- 2009-12-14
- Terminated
- 2009-12-15
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #85871. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.