Reported Aug 2, 2023 · Ongoing
DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs
MEDLINE INDUSTRIES, LP - Northfield
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: MEDLINE INDUSTRIES, LP - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
- DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs
- Lot codes and dates
14 of 14 products
Products covered by this recall # Barcodes Product as published 1 All Lots for series since product launch 2 10193489010671Model Number (Unique Device Identifier) -DYND300010P (Each level packaging: 10193489010671 3 20193489010678Case level packaging: 20193489010678) 4 10193489010688DYND300015P (Each level packaging: 10193489010688 5 20193489010685Case level packaging: 20193489010685) 6 10193489010695DYND300020P (Each level packaging: 10193489010695 7 20193489010692Case level packaging: 20193489010692) 8 1019348901070120193489010708DYND300025P (Each level packaging: 10193489010701 Case level packaging: 20193489010708) 9 10193489010718DYND300030P (Each level packaging: 10193489010718 10 20193489010715Case level packaging: 20193489010715) 11 10193489010725DYND300040P (Each level packaging: 10193489010725 12 20193489010722Case level packaging: 20193489010722) 13 10193489010732DYND300050P (Each level packaging: 10193489010732 14 20193489010739Case level packaging: 20193489010739) - Amount recalled
- 9945 ea
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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