RecallRadar

FDA Drug recall D-0545-2020

Zantac 75 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219

On 2019-12-11 the FDA classified a Class II recall of Zantac 75 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219 by Sanofi Aventis U S, citing CGMP Deviations: Presence of NDMA impurity detected in product.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0545-2020
ClassificationClass II
Statusongoing
Initiated2019-10-22
Published2019-12-11
Last updated2026-09-13 11:52 UTC
CompanySanofi Aventis U S
DistributionUS

Product

Zantac 75 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC's 0597-0122-01 0597-0122-08 0597-0122-13 0597-0122-37 0597-0122-40 0597-0122-54 0597-0122-61 0597-0122-81 0597-0122-96

Reason

CGMP Deviations: Presence of NDMA impurity detected in product.

Identifiers

code_infoall lots

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-0545-2020%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.