Smiths Medical ASD Inc. smiths medical portex, Y' PIECE 15MM, REF 100/276/000 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
smiths medical portex, Y' PIECE 15MM, REF 100/276/000
Brand
Smiths Medical ASD Inc.
Lot Codes / Batch Numbers
UDI/DI 35019315011003, Lot Numbers: 4131841, UDI/DI 35019315022405, Lot Numbers: 4122012, 4133227
Products Sold
UDI/DI 35019315011003, Lot Numbers: 4131841, UDI/DI 35019315022405, Lot Numbers: 4122012, 4133227
Smiths Medical ASD Inc. is recalling smiths medical portex, Y' PIECE 15MM, REF 100/276/000 due to Uncertainty in the seal integrity of the sterile packaging.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Uncertainty in the seal integrity of the sterile packaging.
Recommended Action
Per FDA guidance
Smiths medical issued an URGENT MEDICAL DEVICE CORRECTION notice to its consignees on 07/18/2024 via traceable mailing. The notice explained the issue with the products, potential risk and requested the affected devices be destroyed. Distributors were directed to notify their customers by forwarding the notice. Questions - contact smithsmedical.@sedgwick.com.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026