Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integ
FDA device recall Z-0487-2015 · posted 2014-12-02 · Terminated
Recall details
- Recalling firm
- Beevers Manufacturing & Supply, Inc.
- Reason for recall
- Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.
- Action taken
- Beevers Manufacturing and Supply, Inc. (BMS) of McMinnville, Oregon, began notifying consignees about this recall on 1/18/2007. Customers were advised to inspect blue box that say size 2 (CA 102) and check if size 1 (CA 101) was packed inside. Salter Labs provided BMS' recall report to FDA in October 2014.
- Root cause
- Labeling Change Control
- Status
- Terminated
- Product code
- BZD
- Quantity affected
- 393 units
- Distribution
- Worldwide Distribution: US (nationwide) and country of: ME-Musaffah.
- Date initiated
- 2007-01-18
- Date posted
- 2014-12-02
- Date terminated
- 2014-12-01
- Location
- McMinnville, OR
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