FDA Medical Device Recalls (openFDA)
Terumo Cardiovascular Systems Corp: Heat Exchanger Coil (code Number 0006-0011) used in the ''Custom Cardiovascular Procedure Kits'' .
- Recall number
- Z-0298-03
- Recalling firm
- Terumo Cardiovascular Systems Corp
- Product
- Heat Exchanger Coil (code Number 0006-0011) used in the ''Custom Cardiovascular Procedure Kits'' .
- Status
- Terminated
- Initiated
- 2002-11-07
- Posted
- 2003-04-03
- Terminated
- 2015-08-06
- Reason
- Heat exchanger may contain loose particulate matter
- Root cause
- Other
- Action
- Terumo Cardiovascular Systems notified customers by telephone on 11/8/02 by telephone, fax, and mail to advise distributors and end-users to cease use of the Heat Coil.. A follow-up letter issued to the accounts with instructions for the return of product.
- Quantity
- 10035
- Distribution
- Nationwide. AR, CA, OH, FL, GA, IN, LA, MN, NJ, PA, TN, TX, WA, WI
- Lot, serial or model codes
- TCVS Product code number 0006-00011; all coils in custom cardiovascular procedure kits within their labeled shelf life of 24 months (i.e. kits made 12/1/2000 to 10/25/2002) as follows: Procedure Kit Codes Produced in Lot Lot # 63182-02 CA02 70035; 8539TX CA07 62973; 63153;63688-01; 8539TX CA14 63688-01 CA14T 62973 CA28 8539TX CC04 63688-01; 8525T CC11 63688-01 CC11T 63688-01 CC11TR 62786; 62973;63432; 70060; 63688-01 CC18 63688-01 CC18T 63323-02; 63153 CC25 62336-01; 7957-02; 8525T CD04 63323-02 CD11 70035 ;8539TX; CD18 63182-02; 8525T CD25 62417-03; 62973-01; 63182-02; 63688-01 CE01 63688-01 CE01R 62973-01; 63688-01 CE01T 70187; 62786 CE08 70017; 62973-01 ;63182-02; 63688-01 CE15 63182-02; 63688-01 CE15T 63688-01 CE15TR 70001; 63182-02 CE22 63323-02 CE29 63432; 62336-01; 63079-01; 8525T; 63070-01; 63182-02 CF06 131246-01; 63014-01; 63688-01 CF13 63688-01 CF13R 63688-01 CF13T 70001; 63182-02 CF20 63323-02 CF28 63064 ;62336-01; 62544-01 CG03 63153; 70035; 62973-01 CG10 63064; 62417-03; 62973-01; 63688-01 CG17 63064 CG17R 63079-01; 63688-01 CG24 62336-01 CH01 62786; 63432;62973-01; 63688-01 CH08 62973-01 CH08T 70035; 63323-03; 63688-01 CH15 70001; 63688-01; 63182-02 CH22 63688-01 CH22T 63064; 70001; 70251; 131246-01; 63014-01 CH29 64130; 62544-01; 62973-01 CK05 64130 CK12 64130 CK12T 64130; 63079-01 CK19 63014-01; 63323-03 CK26 70085 CL03 62973-01; 8539TXC CL09 64203; 62973-01; 63064-01 CL16 70413; 8525T CL23 63298 YP04 62417-03 YP11 62336-01 YP18 63014; 8539TX ZA08 62973 ;8539TX ZA22 62973; 63079 ZA29 63432 ZC05 62973; 63014; 63432; 62513-01 ZC12 63014; 63079; 63298; 62973 ZC19 63153 ;63315; 63432; 62361-02; 62513-01 ZC26 62513-01 ZC26T 62786; 63315; 63323 ZD05 63064; 63323; 62544-01; 8525T; 62513-01 ZD12 62361-02; 62544-01; 63323 ZD19 63014 ;8539T; 62786 ZD26 62786; 63315 ZE02 63014; 63064; 63432; 8525T ZE09 63153; 62544-01; 63323 ZE16 62973 ;63323 ZE23 63014 ZE30 63064; 62417-03 ZF07 63064 ZF07R 62786; 63153 ZF14 62544-01; 8539TX ZF21 8539TX ZF21T 8539TX ZF21TR 62973; 63014; 63298 ZF29 62973; 63432; 63315-01 ZG04 62973; 8539TX ZG11 63323; 63079-01 ZG18 63323 ZG18T 62973; 63070; 63432; 62417-03; 63315-01 ZG25 63688; 70001; 63315-01; 8335TX ZH09 62973; 63688; 63079-01; 63153 ZH16 63688; 70001; 62336-01; 8525T ZH23 63688; 70001 ZH23T 63688; 63726; 8539TX ZH30 63688 ZH30R 63688 ZK06 63688 ZK06T 70012 ZK20 63014 ZK20R 70012 ZK20T 62786; 63079-01; 8525T; 8539TX ZK27 8539TX ZK27R 62786; 62973; 63014; 62417-03; 63323-01 ZL04 63014 ZL04R 62973 ZL04T 63014 ZL10 63014 ZL10T 8539TX; 8525T ZL17 62544-01; 63323-01; 8525T ZL24 63323-01 ZL24T 70073 ZM08 62786 ZM15 62786; 62417-03; 8525T ZM22 63014; 63688; 70085; 62336-01; ZM29 70085 ZM29R 62973; 63153; 63432; 63688 ZN05 62973 ZN05T 62973 ZN05TR 8539TX ZN12 8525T ZN19 62417-03; 62544-01 ZN26 62336-01 ;8525T; 63182-02 ZP03 8525T; 63182-02 ZP03T 63064; 63751;63815 ZP10 70106; 63182-02 ZP17
- 510(k) numbers
- ["K000977"]
- PMA numbers
- not on file
- Product code
- DTR
- Firm FEI
- 1000149028
- Firm city
- Ashland
- Firm state
- MA
- 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