Centurion ENT Snuffer Kit Recalled for Incomplete Sterile Package Seals
Centurion Medical Products is recalling 146 units of ENT Snuffer Kits due to incomplete seals that may compromise sterility.
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 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (compromised sterility) where injury has not yet been reported, fitting the High severity criteria.
Plain-English summary
Centurion Medical Products Corporation is recalling 146 units of the Centurion- ENT SNUF3 SNUFFER KIT. The recall is due to incomplete seals on the sterile package, which may compromise the sterility of the device.
The affected product is identified by the lot number 2019011490. The distribution pattern indicates the product was distributed nationwide and to Ghana.
Consumers should stop using the product and contact the recalling firm for further instructions.
The recalled product
- Product
- Centurion- ENT SNUF3 SNUFFER KIT Y
- Manufacturer
- Centurion Medical Products Corporation
- Category
- Medical Device — ENT Devices
- Hazard
- Affected units
- 146
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)
- Product/Description/Lot Numbers: SNUF3 SNUFFER KIT Y 2019011490
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 54 recalled by Centurion Medical Products Corporation under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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