FDA Medical Device Recalls (openFDA)
LivaNova USA Inc.: LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The affected product is a perfusion tubing pack use in surgical procedures requiring extracorporeal support. The perfusion tubing packs include the cuvette used with equipment to monitor blood.
- Recall number
- Z-1389-2020
- Recalling firm
- LivaNova USA Inc.
- Product
- LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The affected product is a perfusion tubing pack use in surgical procedures requiring extracorporeal support. The perfusion tubing packs include the cuvette used with equipment to monitor blood.
- Status
- Terminated
- Initiated
- 2019-07-03
- Posted
- not on file
- Terminated
- 2021-07-09
- Reason
- Perfusion tubing pack was packaged with the incorrect cuvette.
- Root cause
- Employee error
- Action
- On 07/03/2019, the firm contact it customers in person and on 07/08/2019 sent a "MEDICAL DEVICE CORRECTION" Letter informing them of the incorrect cuvette was assembled into Perfusion Pack 046008200 (Lot Number 1912100141) and instructed the customers to: 1. Please check their inventory for PTS pack 046008200, with lot number 1912100141 delivered to their facility; 2. Using the attached Customer Response Form (Attachment 1), please respond by email to USFSN@livanova.com to confirm that they have affected products in their facility; 3. All PTS pack 046008200 with lot number 1912100141 should not be used and should be returned. The Recalling Firm will be contacting its customers to organize the replacement of the affected products. 4. Ensure that this Medical Device Correction is communicated to all personnel within their organization who need to be aware of it. If the customer has transferred any of the affected devices to a third party, please communicate this information to them and inform the LivaNova Quality Assurance Team at USFSN@livanova.com. For questions regarding this Medical Device Correction, please contact us at (800) 986-4702 or by e-mail to USFSN@livanova.com.
- Quantity
- 27 packs
- Distribution
- US Nationwide distribution in the state of IL.
- Lot, serial or model codes
- Model Number: 046008200 Lot Number: 1912100141 UDI: (01)00803622140136(240)046008200 (17)210430(10)1912100141 Cuvette Component P/N 03016 - SAT/HCT B-care 5 cuvette
- 510(k) numbers
- ["K981613"]
- PMA numbers
- not on file
- Product code
- DWE
- Firm FEI
- 1718850
- Firm city
- Arvada
- Firm state
- CO
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28