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Recall Observatory FDA recall evidence

Device product

Elcam Medical MANI 3G Plate BLS RAD B.BRAUN; Manifold for pressure monitoring and intravenous fluid administration. Manufactured by: Elcam Medical ACAL, Israel; Distributed by: Elcam Medical Inc., USA. Sterile

Z-2749-2015

July 19, 2015

Class II

Product summary

Firm
Elcam Medical, Inc.
Event
Event 71880
Status
Terminated
Classification
Class II
Quantity
248,100
Official record key
device-enforcement:Z-2749-2015

Official wording

Reason: Punctured blister packages were detected during the packaging process at the manufacturing site. Potential for device contamination.

Code information: Elcam Part Number: 470306; lot numbers: 1370256602, 1370263901, 370263902, 1370271301, 1370274101, 1470288601, 1470288602, 1470298801, 1470306701, 1470312401 Elcam Part Number: 470307; lot numbers: 1370254802, 1370266801, 370271401, 1370282101, 1470288701, 1470293001, 1470295901 Elcam Part Number: 471601; lot numbers: 1270239001, 1370266601, 1370271501, 1370278801 Elcam Part Number: 471604; lot numbers: 147029310, 1470306801, 1470310201, 1470312501 Elcam Part Number: 477101; lot numbers: 1270244201, 1370278901, 1470292401, 1470292402, 1470298901, 1470301301, 1470306901, 1470310101, 1470312601 Elcam Part Number: 477102; lot numbers: 1370261201, 1570323201 Elcam Part Number: 477901; lot number: 1370255601 Elcam Part Number: 477904; lot number: 1470300101 Elcam Part Number: 478003; lot numbers: 1370261401, 1370266701, 1370271701, 1370271702, 1370278601, 1370278602, 1470293201, 1470296001, 1470307001, 1470312701, 1570316201 Elcam Part Number: 478004; lot numbers: 1370255001, 1370261501, 1370271801, 1370279001, 1470296101, 1470297801, 1470303801, 1470307101, 1470312801 Elcam Part Number: 478701; lot numbers: 1270244901, 1370261301, 1370271901 Elcam Part Number: 478704; lot numbers: 1470296201, 1470299101, 470307201, 1470312901

Distribution pattern: Texas, New Mexico and Pennsylvania

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Punctured blister packages were detected during the packaging process at the manufacturing site. Potential for device contamination.