B Braun Recalls Discofix Stopcock Sets Due to Incorrect Expiration Date
B Braun Medical Inc is recalling specific lots of Discofix Four Way Stopcock Extension Sets because the carton shipper labels display an incorrect expiration date.
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 1/5 (Low).
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class II but involves a documentation error (incorrect expiration date) with no reported injuries or illnesses, fitting the criteria for a Low severity score (packaging/documentation issues).
Plain-English summary
B Braun Medical Inc is recalling specific lots of Discofix Four Way Stopcock Extension Sets, Model/Catalog Number 456025. The recall is due to an incorrect expiration date printed on the carton shipper label.
The affected products are distributed nationwide in the United States and in Canada. The specific lots involved are identified by Lot Numbers 0062062778 and 0062062779, with UDI-DI 04046964183638. The total quantity of units subject to this recall is 25,850.
Consumers and healthcare facilities should check their inventory for these specific lot numbers and model codes. If the products are found, they should be removed from use and returned to the supplier or the manufacturer according to standard recall procedures.
The recalled product
- Product
- Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025
- Manufacturer
- B Braun Medical Inc
- Hazard
- Affected units
- 25,850
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 (3)
- Lot Code: Model No 456025
- UDI-DI 04046964183638
- Lot Numbers 0062062778 and 0062062779
Distribution
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