Spiriva: 5 recalls on record

Recalled by 1 agency: FDA (5).

First recall on record: September 25, 2013. Most recent: January 3, 2024.

Risk classification: Class II: 3 · Class III: 2

Most recent recalls

DateAgencyProduct
January 3, 2024FDASPIRIVA HANDIHALER (tiotropium bromide inhalation powder) 18 mcg/Capsule, 30 capsules, 3 …D-0197-2024
June 2, 2021FDASpiriva HandiHaler (tiotropium bromide inhalation powder) For Oral Inhalation Only 18 mcg…D-0453-2021
February 7, 2018FDASPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90 capsules (u…D-0242-2018
April 16, 2014FDASpiriva HandiHaler (tiotropium bromide inhalation powder), Do Not Swallow Spiriva Capsule…D-1230-2014
September 25, 2013FDASPIRIVA HandiHaler (Tiotropium Bromide Inhalation Powder) Capsules 18 mcg per dose, Rx on…D-1057-2013

Questions about this brand

How many recalls does Spiriva have?
Recalert has 5 U.S. recalls on record for Spiriva, published between September 25, 2013 and January 3, 2024.
What was the most recent Spiriva recall?
FDA recall D-0197-2024, published January 3, 2024: SPIRIVA HANDIHALER (tiotropium bromide inhalation powder) 18 mcg/Capsule, 30 capsules, 3 blister cards, each card contains 10 capsules, Rx only, For oral inhalation only, Distributed by: Boehringer I…
Which agencies have recalled Spiriva products?
Spiriva products appear in recalls from: FDA (5).

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