Medical DeviceApr 26, 2017
Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w gxl:w1/r rbls recall — FDA Z-1869-2017
The stopcock was found to have punctures.
Class IIFDA: TerminatedElcam Medical, Inc.
Recall history in this database
Classification mix: Class II: 3.
Medical DeviceSep 16, 2015
Elcam Medical MANI 3G Plate BLS RAD B.BRAUN recall — FDA Z-2749-2015
Punctured blister packages were detected during the packaging process at the manufacturing site. Potential for device contamination.
Class IIFDA: TerminatedElcam Medical, Inc.
Medical DeviceSep 16, 2015
Elcam Medical Minimal Residual Volume Luer activated Swabbable stopcock (MRVLS) for pressure recall — FDA Z-2748-2015
Punctured blister packages were detected during the packaging process at the manufacturing site. Potential for device contamination.
Class IIFDA: TerminatedElcam Medical, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Elcam Medical, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.