B. Braun Recalls Y-Type Blood Sets Due to Leakage Risk
B. Braun Medical is recalling 5,616 Y-Type Blood Sets because of a potential for leakage at the joint between the blood filters and tubing.
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 involves a medical device with a risk of harm (leakage) where no specific injuries or illnesses have been reported in the source text, fitting the criteria for a High severity score.
Plain-English summary
B. Braun Medical, Inc. is recalling 5,616 units of Y-Type Blood Sets, Catalog Number 490314. The recall is due to a potential for leakage at the joint between the blood filters and tubing.
The affected products were distributed nationwide in the United States. The recall includes specific lot numbers with expiration dates ranging from April 30, 2022, to June 30, 2022.
Healthcare providers and consumers should stop using the affected blood sets and contact B. Braun Medical for further instructions or a replacement.
The recalled product
- Product
- Y-Type Blood Set, Catalog Number 490314
- Manufacturer
- B. Braun Medical, Inc.
- Hazard
- Affected units
- 5,616
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 (5)
- GUIDID: 04046964527180 Lot Numbers: 61674868 - Expiration Date April 30
- 2022
- 61677175 - Expiration Date April 30
- 61678259 - Expiration Date May 31
- 61685087 - Expiration Date June 30
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 7 recalled by B. Braun Medical, Inc. 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.
See all 7 products in this recall →Related recalls
Same manufacturer · B. Braun Medical, Inc.
See all →- SevereB. Braun Recalls Lactated Ringer's Injection Due to Particulate Matter
FDA (Drugs) · 2026-09-02
- ModerateB. Braun UPMC double catheter trays contain Mastisol with cracking tubing
FDA (Devices) · 2026-06-10
- ModerateB. Braun Shands kits contain Mastisol adhesive with cracking tubing
FDA (Devices) · 2026-06-10
- ModerateB. Braun spinal epidural kits contain Mastisol with cracking tubing
FDA (Devices) · 2026-06-10
- ModerateB. Braun kits contain Mastisol adhesive with potentially cracking tubing
FDA (Devices) · 2026-06-10
Same hazard · leakage
See all →- HighConvaTec Esteem Body Soft Convex Urostomy Pouches Recalled for Leakage
FDA (Devices) · 2026-08-26
- SevereStryker AHTO Tube Set Packaging Recalled for Handpiece Leaking
FDA (Devices) · 2026-08-12
- SevereMedtronic Perfusion Systems Recalls EOPA Elongated One-Piece Arterial Cannula Model 77522
FDA (Devices) · 2026-08-05
- HighICU Medical Recalls Hotline Fluid Warming Sets Due to Leakage Risk
FDA (Devices) · 2026-07-29
- SevereABIOMED Introducer Kit 23 Fr heart pump accessory leakage risk
FDA (Devices) · 2026-07-22