Reported Dec 10, 2014 · Terminated
Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an…
Beevers Manufacturing & Supply, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Beevers Manufacturing & Supply, Inc. · 850 SW Booth Bend Rd · McMinnville, OR · 97128-9320
Is this the product you have?
- Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integral hook strip (i.e., Velcro) to allow for the use of a loop material to help secure a nasal interface. The Cannulaide is applied under and over the nose of infants to provide a protective barrier to the philtrum, columella, septum, nares, and tip of nose. It is available in multiple sizes that vary the external geometry and nare hole size and spacing to allow for use on infants ranging from less than 700 grams to greater than 3000 grams. It is a non sterile, single patient use, disposable device.
- Lot codes and dates
- Lot 20060928. Product expired in 2009.
- Amount recalled
- 393 units
Where it was sold
- Nationwide
- ME
Why it was recalled
Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.
This product could cause temporary or reversible health problems — stop using it.
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