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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