FDA Medical Device Recalls (openFDA)
Hospira Inc.: Angiographic Syringe, 12 cc Thumb Ring with Rotator Reservoir.
- Recall number
- Z-0618-05
- Recalling firm
- Hospira Inc.
- Product
- Angiographic Syringe, 12 cc Thumb Ring with Rotator Reservoir.
- Status
- Terminated
- Initiated
- 2004-11-02
- Posted
- 2005-03-15
- Terminated
- 2005-07-25
- Reason
- Syringes could possibly allow air to enter the patient's vascular system.
- Root cause
- Other
- Action
- Consignees were notified by letter on 11/10/04 or by telephone on 11/11/04.
- Quantity
- 8175 syringes
- Distribution
- Domestic distribution: Nationwide, including 2 military/VA facilities. International distribution: Spain, Belgium, Greece, Japan, and France.
- Lot, serial or model codes
- List Numbers: 4204201 Lot Numbers: 13193SN; 15171SN; 17151SN
- 510(k) numbers
- ["K884823","K932188","K933700","K942329"]
- PMA numbers
- not on file
- Product code
- DQO
- Firm FEI
- 3013319212
- Firm city
- Lake Forest
- Firm state
- IL
- 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