RecallRadar

FDA Device recall Z-0993-2013

Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion of insulin for the treat…

On 2013-04-10 the FDA classified a Class I recall of Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion of insulin for the treat… by Animas, citing animas has identified a component issue affecting a small supply of the Animas(R) 2020 insulin pumps. The component issue may trigger the pumps to sound a false alarm or warning r….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0993-2013
ClassificationClass I
Statusterminated
Initiated2013-01-03
Published2013-04-10
Last updated2026-09-13 11:53 UTC
CompanyAnimas
DistributionUS

Product

Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is indicated for continuous subcutaneous infusion of insulin for the treatment of insulin-requiring diabetes.

Reason

Animas has identified a component issue affecting a small supply of the Animas(R) 2020 insulin pumps. The component issue may trigger the pumps to sound a false alarm or warning related to one of the following: - Loss of prime; -Occlusion; or -No cartridge detected.

Identifiers

code_info
Part Numbers 101370-00, 101371-00, 101372-00, 101374-00, 101375-00, 100380-00, 100381-00, 100382-00, 100384-00, and 100…Part Numbers 101370-00, 101371-00, 101372-00, 101374-00, 101375-00, 100380-00, 100381-00, 100382-00, 100384-00, and 100385-00. Serial Numbers: 62-00202-12 36-97839-12 01-05118-12 25-02849-12 63-99894-12 80-00093-12 37-04692-12 92-04130-12 27-99281-12 32-99198-12 81-00513-12 44-02998-12 46-99680-12 23-02928-12 03-04500-12 01-03079-12 79-00261-12 26-99273-12 16-03650-12 93-03219-12 12-02808-12 21-04715-12 34-98485-12 40-98917-12 19-03646-12 27-00988-12 09-02900-12 28-99437-12 96-05032-12 03-00908-12 25-98448-12 15-02913-12 33-99713-12 91-00632-12 71-01130-12 07-05064-12 15-00948-12 92-02246-12 36-98399-12 97-00740-12 75-00229-12 32-01986-12 80-02118-12 97-04135-12 26-00899-12 20-03654-12 44-99495-12 31-99285-12 23-01970-12 43-99575-12 48-99499-12 83-00191-12 11-00768-12 31-99461-12 88-02066-12 88-00189-12 34-02974-12 24-02950-12 54-99790-12 96-03067-12 91-04122-12 74-00235-12 23-02759-12 96-04127-12 11-02652-12 44-994

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0993-2013%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.