Medline Industries, Lp: Circuit, Breathing (w Connector, Adaptor, Y Piece)
Recall Summary Two Medline anesthesia convenience kits (model numbers DYNJ905503F and DYNJ905503G) are recalled due to quality issues with anesthetic medications included in them. The anesthetic drugs—Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection—were found to have problems during an FDA inspection of the supplier. These kits have been distributed nationwide across all U.S. states and the District of Columbia.
- Recalling firm
- Medline Industries, LP
- Product
- Medline Convenience Kits: 1) DYNJ905503F, Model Number: CV ANESTHESIA - ROOM SET UP; 2) DYNJ905503G, Model Number: CV ANESTHESIA - ROOM SET UP
- Reason
- The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
- Classification
- Class I
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-05-06
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/bfd796d5-d112-421a-8a99-28ec4d1a43da