PlainRecalls
FDA Drug Moderate Class II Terminated

lidocaine 2%, 100 mg /5 mL, (20 mg/mL), 5 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6006-1

Reported: August 9, 2023 Initiated: July 17, 2023 #D-1074-2023

Product Description

lidocaine 2%, 100 mg /5 mL, (20 mg/mL), 5 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6006-1

Reason for Recall

Lack of assurance of sterility: Lack of validation data for sanitization cycles

Details

Units Affected
9,517 syringes
Distribution
Nationwide in the USA
Location
San Diego, CA

Frequently Asked Questions

What product was recalled?
lidocaine 2%, 100 mg /5 mL, (20 mg/mL), 5 mL Syringe, Rx only, CAPS, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-6006-1. Recalled by Central Admixture Pharmacy Services Inc. Units affected: 9,517 syringes.
Why was this product recalled?
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Which agency issued this recall?
This recall was issued by the FDA Drug on August 9, 2023. Severity: Moderate. Recall number: D-1074-2023.