Cannulaide recall
Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integral hook strip (i.e., Velcro)…
Why was Cannulaide recalled?
Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot 20060928. Product expired in 2009.
- Product
- Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integral hook strip (i.e., Velcro)…
- Recalling firm
- Beevers Manufacturing & Supply, Inc.
- Quantity
- 393 units
- Distribution
- Worldwide Distribution: US (nationwide) and country of: ME-Musaffah.
- Recall date
- December 10, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)