PlainRecalls
FDA Devices Moderate Class II Ongoing

DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs

Reported: August 2, 2023 Initiated: March 28, 2023 #Z-2227-2023

Product Description

DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs

Reason for Recall

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.

Details

Units Affected
9945 ea
Distribution
Worldwide distribution - US Nationwide and the country of Bermuda.
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 9945 ea.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 2, 2023. Severity: Moderate. Recall number: Z-2227-2023.