Centurion Medical Products Recalls Nosebleed Kits Containing Major Nasal Spray
Centurion Medical Products is recalling 30 Nosebleed Tray kits (Kit Code MNS3885) distributed in Connecticut and Illinois because they contain Major Nasal Decongestant Spray.
What this means for you
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 is classified as FDA Class II, and the source text does not explicitly state that no illnesses or injuries have been reported. Per the rubric, risk-of-harm products where injury has not yet been reported are classified as High.
Plain-English summary
Centurion Medical Products Corporation is recalling 30 Nosebleed Tray kits, identified by Kit Code MNS3885. The recall affects two specific lots: Lot # 2018121780 (Expiration 08/31/2020) and Lot # 2018111280 (Expiration 05/31/2020). These kits were distributed in Connecticut and Illinois.
The recall was initiated because the medical device kits contain Major Nasal Decongestant Spray. The source text does not specify the exact nature of the defect or the specific health risk associated with the presence of this spray in the kits.
Consumers and healthcare facilities in the affected areas should check their inventory for these specific lot numbers and expiration dates. If found, the kits should be removed from use and returned to the manufacturer or disposed of according to local regulations. The source text does not provide specific contact information for the recall.
The recalled product
- Product
- NOSEBLEED TRAY Kit Code: MNS3885
- Manufacturer
- Centurion Medical Products Corporation
- Category
- Medical Device — Nosebleed Kit
- Hazard
- Affected units
- 30
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 # 2018121780 Exp 08/31/2020 Lot # 2018111280 Exp 05/31/2020
Distribution
Part of a larger recall action
This product is one of 3 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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