RecallRadar

FDA Drug recall D-0229-2026

Lidocaine HCI 2% and Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton containing 50 single-dose Ca…

On 2025-12-24 the FDA classified a Class II recall of Lidocaine HCI 2% and Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton containing 50 single-dose Ca… by Novocol Pharmaceutical, citing defective container: cracked/broken cartridges.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0229-2026
ClassificationClass II
Statusongoing
Initiated2025-10-31
Published2025-12-24
Last updated2026-09-13 11:52 UTC
CompanyNovocol Pharmaceutical
DistributionUS

Product

Lidocaine HCI 2% and Epinephrine 1:100,000 (Lidocaine HCI and Epinephrine Injection USP), packaged in a carton containing 50 single-dose Cartridges, 1.7 ml each, Rx only, Manufactured for Patterson Dental Supply, Inc., 1031 Mendota Heights Road, Saint Paul, MN55120, Manufactured by: Novocol Pharmaceutical of Canada, Inc., NDC 50227-1030-5.

Reason

Defective container: cracked/broken cartridges

Identifiers

ndc50227-1030-5
code_infoLot: D05362A, expires: 07-31-2027

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0229-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.