RecallRadar

FDA Drug recall D-019-2014

Cetacaine Liquid Topical Anesthetic, Rx Only, a) 14 g bottle (NDC 10223-0202-2)

On 2013-12-04 the FDA classified a Class II recall of Cetacaine Liquid Topical Anesthetic, Rx Only, a) 14 g bottle (NDC 10223-0202-2) by Cetylite Industries, citing subpotent Drug: Cetacaine Topical Anesthetic Liquid is being recalled because one of the three active ingredients, tetracaine, is below the specification limit at the 21 month sta….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-019-2014
ClassificationClass II
Statusterminated
Initiated2013-04-02
Published2013-12-04
Last updated2026-09-13 11:51 UTC
CompanyCetylite Industries
DistributionUS

Product

Cetacaine Liquid Topical Anesthetic, Rx Only, a) 14 g bottle (NDC 10223-0202-2); Kit w/14 g (NDC 10223-0202-3); 30 g bottle (NDC 10223-0202-4) Manufactured by Cetylite Industries, Inc., 9051 River Road Pennsauken, NJ 08110 -

Reason

Subpotent Drug: Cetacaine Topical Anesthetic Liquid is being recalled because one of the three active ingredients, tetracaine, is below the specification limit at the 21 month stability test point.

Identifiers

ndc10223-0202-2
ndc10223-0202-4
ndc10223-0202-5
ndc10223-0202-6
ndc10223-0202-7
ndc10223-0202-8
ndc10223-0225-1
ndc10223-0226-1
ndc10223-0202-3
code_infoLot 470 exp. 04/13, 471 exp. 06/13, 472 exp. 10/13

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-019-2014%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.