D-0229-2026 Class II Ongoing

Recalled by Novocol Pharmaceutical Of Canada, Inc. — Cambridge

FDA drug recall D-0229-2026 was initiated by Novocol Pharmaceutical Of Canada, Inc. on Oct 31, 2025 and is designated Class II. Reason for recall: Defective container: cracked/broken cartridges The recall status is ongoing. Affected quantity: 12,033 cartons.

Recall details

Product Type
Drugs
Report Date
Dec 24, 2025
Initiation Date
Oct 31, 2025
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
12,033 cartons

Product description

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 for recall

Defective container: cracked/broken cartridges

Distribution pattern

U.S.A. Nationwide

Code information

Lot: D05362A, expires: 07-31-2027

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-0229-2026
openFDA file date
Nov 10, 2026
Loaded by RegDataLab
Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for D-0229-2026. Report a data issue: hello@regdatalab.com.