MEDLINE INDUSTRIES, LP Northfield DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs
Brand
MEDLINE INDUSTRIES, LP Northfield
Lot Codes / Batch Numbers
All Lots for series since product launch, Model Number (Unique Device Identifier) -DYND300010P (Each level packaging: 10193489010671, Case level packaging: 20193489010678), DYND300015P (Each level packaging: 10193489010688, Case level packaging: 20193489010685), DYND300020P (Each level packaging: 10193489010695, Case level packaging: 20193489010692), DYND300025P (Each level packaging: 10193489010701 Case level packaging: 20193489010708), DYND300030P (Each level packaging: 10193489010718, Case level packaging: 20193489010715), DYND300040P (Each level packaging: 10193489010725, Case level packaging: 20193489010722), DYND300050P (Each level packaging: 10193489010732, Case level packaging: 20193489010739)
Products Sold
All Lots for series since product launch; Model Number (Unique Device Identifier) -DYND300010P (Each level packaging: 10193489010671; Case level packaging: 20193489010678); DYND300015P (Each level packaging: 10193489010688; Case level packaging: 20193489010685); DYND300020P (Each level packaging: 10193489010695; Case level packaging: 20193489010692); DYND300025P (Each level packaging: 10193489010701 Case level packaging: 20193489010708); DYND300030P (Each level packaging: 10193489010718; Case level packaging: 20193489010715); DYND300040P (Each level packaging: 10193489010725; Case level packaging: 20193489010722); DYND300050P (Each level packaging: 10193489010732; Case level packaging: 20193489010739)
MEDLINE INDUSTRIES, LP Northfield is recalling DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs due to The case and each (i.e. packet) labels for the DYND3000xxP series do not include an expiration date, however, the lubricating jelly (MDS032280) includ. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The case and each (i.e. packet) labels for the DYND3000xxP series do not include an expiration date, however, the lubricating jelly (MDS032280) included in the DYNDP3000xxP series is labeled with an expiration date.
Recommended Action
Per FDA guidance
The consignee recall notification was sent out via first class mail and email on 03/28/2023. The letter instructs the consignee to over-label the Flexible Laryngeal Mask Airway Packs stating to Check the Expiration date of Lubricating Jelly MDS032280 and do not use if Expired . No product is to be returned back to Medline Industries, LP.
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