Centurion brand CirClamp with 1.3 cm bell, sterile, single… recallZ-0836-05 · Tri-State Hospital Supply Corp · initiated Apr 12, 2005
Terminated All recalls posted in May 2005
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Tri-State Hospital Supply Corp or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Lot 11224 may contain a 1.1 cm clamp and bell and neither lot is labeled as reprocessed, when they have been reprocessed.
FDA root cause category: Other
What the company is doing
Consignees were notified to return the product via letter dated 4/12/05.
Recall details
- Recall number
- Z-0836-05
- Recall class
- Not yet classified by the FDA
- Status
- Terminated
- Initiated by the company
- Apr 12, 2005
- Posted by the FDA
- May 12, 2005
- Recalling firm
- Tri-State Hospital Supply Corp
- Quantity
- 4078
- Product code
- HFX
- FDA submissions
- K890897
- Distribution
- Nationwide.
Product description
Centurion brand CirClamp with 1.3 cm bell, sterile, single use; product 330.
Code information (models, lots, serial numbers)
Lots 11224 and 06284.
Other devices under the same FDA submission
15 devices cleared under K890897 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
- Centurion CR230KCenturion Medical Products Corporation · CLAMP, CIRCUMCISION2 recalls0 reports
- Centurion CR3145KCenturion Medical Products Corporation · CLAMP, CIRCUMCISION2 recalls0 reports
- Centurion 330CRKCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall8 reports
- Centurion 310CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall4 reports
- Centurion 330CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall1 report
- Centurion 210CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
- Centurion 230CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
- Centurion 245CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
- Centurion 3145CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
- Centurion 345CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
- Centurion 200CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
- Centurion 310CRKCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 31645).
- Z-0837-05 · TerminatedCenturion brand CirClamp with 1.1 cm bell, sterile, single use; product 310.
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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