Atlas FDA

Milex 60cc Handy-Vak Locking Syringe Ref: MX500

FDA device recall Z-0401-06 · posted 2006-01-18 · Terminated

Recall details

Recalling firm
CooperSurgical, Inc.
Reason for recall
Potential for the plunger to separate from the piston
Action taken
CooperSurgical notified consignees by telephone and follow-up letter dated 11/3/05 via fax. Accounts are requested to discontinue use and return inventory.
Root cause
Other
Status
Terminated
Product code
FMF
Quantity affected
496 units
Distribution
CA, CO, HI, IL, MA, NH, PA, VA, WA Foreign: Canada
Date initiated
2005-11-01
Date posted
2006-01-18
Date terminated
2012-05-14
Location
Trumbull, CT

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