FDA Drug Recalls
Class I
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Firms
/ Boehringer Ingelheim Pharmaceuticals, Inc.
Boehringer Ingelheim Pharmaceuticals, Inc.
12 FDA drug recalls on record.
Date
Class
Drug
Status
2023-03-09
Class II
Jardiance
Terminated
2021-05-04
Class II
Micardis
Terminated
2020-10-05
Class II
Catapres (clonidine hydrochloride, USP) 0.2 mg, tablet, 100-count bottle, Rx only, Dist.
Terminated
2020-10-05
Class II
Catapres (clonidine hydrochloride, USP) 0.1 mg, tablet, 100-count bottle, Rx only, Dist.
Terminated
2020-10-05
Class II
Catapres (clonidine hydrochloride, USP) 0.3 mg, tablet, 100-count bottle, Rx only, Dist.
Terminated
2019-03-07
Class III
Mirapex (pramipexole dihydrochloride) Tablets, 1 mg, 100-count unit-dose tablets per foldi
Terminated
2018-10-22
Class II
Catapres .2 (clonidine hydrochloride, USP) 0.2mg, 100-count bottles, Rx only, Dist. by: Bo
Terminated
2018-09-04
Class II
Synjardy
Terminated
2017-12-14
Class II
Spiriva
Terminated
2017-09-22
Class III
Mobic (meloxicam) tablets, 15 mg, package in 100-count bottle, Rx only, Dist. by: Boehring
Terminated
2016-10-06
Class II
DIPYRIDAMOLE Tablets USP, 75 mg, 100-count bottle, Rx only, Dist. by: Roxane Laboratories,
Terminated
2016-10-06
Class II
Persantine (dipyridamole USP) tablets, 75 mg, 100-count bottles, Rx only, Dist. by: Boehri
Terminated