MEDLINE INDUSTRIES, LP Northfield Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box 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
Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box
Brand
MEDLINE INDUSTRIES, LP Northfield
Lot Codes / Batch Numbers
Medline Item Number and Lot(s): 1) DYND290010, Lot 63521050001 (UDI: 10193489036688) 2) DYND290015, Lot 63521050001 (UDI: 10193489036695) 3) DYND290020, Lots 63521050001, 63521110001, and 63521100002 (UDI: 10193489036701) 4) DYND290025, Lots 63521050001, 63521110001, and 63521100002 (UDI: 10193489036718) 5) DYND290030, Lots 63521050001, 63521100002, 63521050002, and 63521110001 (UDI: 10193489036725) 6) DYND290040, Lots 63521050001, 63521100002, 63521050002, and 63521110001 (UDI: 10193489036732) 7) DYND290050, Lots 63521050001, 63521110001, and 63521100002 (UDI: 10193489036749)
Products Sold
Medline Item Number and Lot(s): 1) DYND290010; Lot 63521050001 (UDI: 10193489036688) 2) DYND290015; Lot 63521050001 (UDI: 10193489036695) 3) DYND290020; Lots 63521050001, 63521110001, and 63521100002 (UDI: 10193489036701) 4) DYND290025; Lots 63521050001, 63521110001, and 63521100002 (UDI: 10193489036718) 5) DYND290030; Lots 63521050001, 63521100002, 63521050002, and 63521110001 (UDI: 10193489036725) 6) DYND290040; Lots 63521050001, 63521100002, 63521050002, and 63521110001 (UDI: 10193489036732) 7) DYND290050; Lots 63521050001, 63521110001, and 63521100002 (UDI: 10193489036749)
MEDLINE INDUSTRIES, LP Northfield is recalling Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box due to The mask cuff may disconnect from the device's breathing tube.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The mask cuff may disconnect from the device's breathing tube.
Recommended Action
Per FDA guidance
Medline Industries, Inc. notified all affected consignees via first class mail on March 8, 2022. Medline Industries, LP. has provided each consignee with a letter and a Destruction form to record their response to the recall notification. Each Response received will be recorded and Medline Industries, LP. will send subsequent letters to consignees that have not provided a response to our recall notification in the allotted time. Each consignee was provided with a destruction form to complete and return. The consignees are responsible to destroy their product per their local and state regulations. No product will be returned to be stored.
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