RecallRadar

FDA Drug recall D-1200-2016

LIDOCAINE 2% (PF) IN NACL, 10ML Vials, MEDAUS PHARMACY

On 2016-07-20 the FDA classified a Class II recall of LIDOCAINE 2% (PF) IN NACL, 10ML Vials, MEDAUS PHARMACY by Medaus, citing lack of Assurance of Sterility.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1200-2016
ClassificationClass II
Statusterminated
Initiated2016-05-13
Published2016-07-20
Last updated2026-09-13 11:51 UTC
CompanyMedaus
DistributionUS

Product

LIDOCAINE 2% (PF) IN NACL, 10ML Vials, MEDAUS PHARMACY

Reason

Lack of Assurance of Sterility

Identifiers

code_info
Lot #: 151203-48, BUD: 05/31/16; Lot #: 151204-9, BUD: 06/01/16; Lot #: 151218-20, BUD: 06/15/16; Lot #: 160125-23,…Lot #: 151203-48, BUD: 05/31/16; Lot #: 151204-9, BUD: 06/01/16; Lot #: 151218-20, BUD: 06/15/16; Lot #: 160125-23, BUD: 07/23/16; Lot #: 160125-24, BUD: 07/23/16; Lot #: 160125-25, BUD: 07/23/16; Lot #: 160127-6, BUD: 07/25/16; Lot #: 160302-76, BUD: 08/29/16; Lot #: 160302-77, BUD: 08/29/16

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-1200-2016%22

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