Beevers Cannulaide Model 101 Recalled for Incorrect Labeling
Beevers Manufacturing recalled 393 units of Cannulaide Model 101 because the product was packed and labeled as Model 102.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the specific defect is a minor labeling error (wrong model number) with no reported injuries or illnesses, fitting the criteria for a moderate severity score.
Plain-English summary
Beevers Manufacturing & Supply, Inc. is recalling 393 units of Cannulaide, Model 101. The recall was initiated because the firm discovered that the Model 101 product was packed and labeled as Model 102.
The Cannulaide is a non-sterile, single-patient use, disposable medical device applied under and over the nose of infants to provide a protective barrier. The affected units are from Lot 20060928 and expired in 2009. The product was distributed worldwide, including nationwide in the US and in Musaffah.
Consumers and healthcare providers should stop using the affected units and contact the recalling firm for instructions on return or disposal.
The recalled product
- Product
- 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…
- Manufacturer
- Beevers Manufacturing & Supply, Inc.
- Hazard
- Affected units
- 393
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot 20060928. Product expired in 2009.
Distribution
Distributed nationwide across the United States.
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