FDA Medical Device Recalls (openFDA)
Roche Diagnostics Operations, Inc.: Roche cobas 8000 modular analyzer series (i.e., cobas 8000 ISE module; cobas c 502, 701, and 702 modules; and cobas e 602 and 801 modules). Chemistry Analyzer (photometric discrete), for clinical use Part Number: 08763662001
- Recall number
- Z-0754-2021
- Recalling firm
- Roche Diagnostics Operations, Inc.
- Product
- Roche cobas 8000 modular analyzer series (i.e., cobas 8000 ISE module; cobas c 502, 701, and 702 modules; and cobas e 602 and 801 modules). Chemistry Analyzer (photometric discrete), for clinical use Part Number: 08763662001
- Status
- Open, Classified
- Initiated
- 2020-12-08
- Posted
- not on file
- Terminated
- not on file
- Reason
- Potential for Changed Configuration Settings on the cobas 8000 modular analyzer series/cobas pro integrated solutions, may cause incorrect results in several affected parameters. In the case of poor sample quality, discrepant results may remain undetected due to the absence of associated data flags.
- Root cause
- Software design
- Action
- Roche recall issued Urgent Medical Device Correction (UMDC TP-01165 and UMDC TP-01169) notifications on 12/8/2020 via UPS Ground (receipt required). Both UMDCs will also be posted to the diagnostics.roche.com website. Letter states reason for recall, health risk and action to take: Consignee Instructions: Inform any operators who use the cobas 8000 modular analyzer series or the cobas pro integrated solutions of the potential hazards associated with this issue and provide a copy of the UMDC notification, as appropriate. Follow the actions outlined in the Customer Actions to Determine if the Issue Has Occurred section of the UMDC. Confirm that you have backed up your most recent settings. Repeat this maintenance function whenever a system setting is changed. Consult with the physician or pathologist at your facility to determine specific clinical implications for your patients. Complete the enclosed faxback form and return it following the instructions on the form. File this UMDC for future reference. Contact the Roche Support Network Customer Support Center, 24 hours a day, seven days a week at 1-800-428-2336 if you have questions about the information contained in this UMDC.
- Quantity
- 1050 units
- Distribution
- US Nationwide distribution.
- Lot, serial or model codes
- Serial No. 1017-01 1017-04 1019-09 1019-09 1019-09 1020-01 1022-05 1022-05 1029-09 1029-09 1030-08 1030-09 1030-09 1030-10 1034-09 1036-07 1036-07 1138-03 1138-03 1138-04 1140-09 1140-10 1142-01 1142-02 1142-02 1142-04 1142-04 1142-05 1142-06 1142-08 1142-08 1142-08 1142-09 1142-09 1142-09 1142-10 1143-01 1143-06 1143-09 1143-09 1143-10 1144-01 1146-02 1147-01 1147-03 1147-04 1147-07 1147-09 1149-01 1150-04 1150-05 1150-06 1150-06 1150-06 1150-06 1150-06 1161-05 1161-06 1161-08 1161-08 1161-08 1161-08 1161-08 1163-07 1163-07 1163-07 1163-07 1163-07 1163-10 1163-10 1164-01 1167-06 1167-06 1167-06 1167-07 1167-07 1167-08 1167-08 1167-09 1167-09 1167-10 1167-10 1168-02 1168-02 1168-02 1168-03 1168-03 1168-03 1168-03 1168-03 1168-03 1168-03 1168-03 1168-04 1168-04 1171-01 1171-01 1171-01 1171-02 1171-05 1206-02 1206-03 1206-04 1206-05 1206-05 1206-06 1206-06 1206-06 1206-06 1206-07 1207-07 1207-08 1207-08 1207-08 1207-09 1207-09 1214-17 1214-18 1214-19 1214-19 1214-19 1214-19 1214-19 1214-20 1214-20 1214-20 1215-01 1215-01 1215-01 1215-17 1215-17 1215-17 1215-18 1215-20 1215-20 1215-20 1215-20 1216-18 1216-18 1325-01 1325-02 1325-03 1325-13 1325-13 1325-13 1325-14 1325-14 1325-14 1325-14 1325-14 1325-15 1325-16 1326-01 1326-01 1326-01 1326-02 1326-02 1326-02 1326-03 1326-03 1326-03 1326-04 1326-13 1326-14 1326-15 1326-16 1326-17 1326-17 1326-17 1326-18 1326-19 1326-19 1326-19 1326-20 1332-01 1332-01 1332-02 1332-02 1332-03 1332-06 1332-13 1332-14 1332-15 1332-16 1343-10 1344-01 1344-02 1344-03 1344-04 1344-05 1344-05 1344-05 1344-05 1344-06 1344-07 1344-08 1344-09 1344-09 1344-09 1344-10 1344-10 1344-10 1345-01 1345-03 1345-04 1345-05 1345-05 1350-06 1350-06 1350-07 1350-08 1351-02 1353-01 1353-02 1353-03 1353-03 1353-04 1353-04 1360-02 1360-02 1360-02 1360-03 1360-03 1360-03 1360-04 1361-05 1361-06 1361-06 1361-06 1361-09 1361-09 1361-10 1361-10 1362-01 1362-02 1362-03 1362-04 1362-04 1362-04 1362-04 1362-04 1362-05 1362-05 1364-02 1364-03 1364-04 1364-05 1364-06 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15H6-06 15K9-08 15K9-09 15L0-02 15L9-09 15M6-07 15M6-09 15M6-10 15M7-01 15M7-02 15M7-03 15M7-03 15M7-04 15M7-04 15M7-05 15M7-05 15M7-06 15M7-06 15M9-03 15M9-04 15M9-07 15P0-02 15P2-08 15P5-03 15P5-03 15P5-04 15P5-04 15P6-03 15P6-03 15P8-09 15P8-10 15P9-01 15P9-01 15P9-02 15P9-02 15P9-03 15P9-05 15P9-06 15P9-07 15P9-07 15P9-08 15R8-01 15R8-01 15R8-04 15R8-04 15R8-05 15R8-06 15R8-07 15R8-10 15R8-10 15R9-01 15R9-02 15R9-03 15R9-04 15R9-05 15R9-06 15S3-03 15S3-04 15S3-08 15S3-10 1638-09 1639-01 1639-02 1639-03 1639-06 1639-07 1639-08 1639-09 1639-10 1640-01 1645-03 1647-09 1647-10 1647-10 1648-01 1648-01 1648-02 1648-03 1648-04 1648-05 1648-06 1648-07 1655-06 1655-07 1656-01 1656-02 16S8-03 16S8-04 16S8-05 16S8-07 16S8-08 16S8-09 16S9-01 16S9-02 16S9-02 16S9-03 16S9-03 16S9-04 16S9-05 16S9-08 16S9-08 16U1-05 16U1-09 16U1-10 16U2-01 16U2-02 16U2-03 16U2-04 16U2-09 16U2-10 16U5-02 16U5-03 16U5-04 16U5-10 16U6-01 16U6-01 16U6-02 16U6-02 16U6-03 16U6-05 16U6-06 16U6-07 16V9-03 16W0-06 16W0-07 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20M0-06 20M0-06 20M0-06 20M0-06 20M0-07 20M0-08 20M0-09 20M0-10 20M1-01 20M5-09 20M5-10 20M6-01 20M6-02 20M6-09 20M6-10 20P1-09 20P1-10 20P2-01 20P2-02 20P2-03 20P2-05 20P2-06 20P2-07 20P2-08 20P3-03 20P3-04 20P7-02 20P7-03 20P7-04 20P7-05 20P7-06 20P7-07 20P7-08 20R1-06 20R1-07 20R1-08 20R1-09 20R2-09 20R7-03 20S1-03 20S1-04 20S1-05 20S3-06 20S3-06 20S3-06 20S3-06 20S3-07 20S3-08 20S3-09 20S7-02 20S7-03 20S7-04
- 510(k) numbers
- ["K100853"]
- PMA numbers
- not on file
- Product code
- JJE
- Firm FEI
- 1823260
- Firm city
- Indianapolis
- Firm state
- IN
- 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