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Smisson-Cartledge Biomedical, LLC recalls

Every recall we track for Smisson-Cartledge Biomedical, LLC — 3 in all, all from 2021 — plus the complaints and injury reports the public filed about them.

3recalls

Recalls per year, by danger level

Recalls from Smisson-Cartledge Biomedical, LLC peaked in 2021 (3); 3 since 2017.

2017: 0 recalls20172018: 0 recalls20182019: 0 recalls20192020: 0 recalls20202021: 3 recalls — 3 lower risk320212022: 0 recalls20222023: 0 recalls20232024: 0 recalls20242025: 0 recalls20252026 (to date): 0 recalls2026to date

All FDA recall records for Smisson-Cartledge Biomedical, LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for Smisson-Cartledge Biomedical, LLC, by danger level
YearStop using nowUse cautionLower riskNot yet ratedTotal
201700000
201800000
201900000
202000000
202100303
202200000
202300000
202400000
202500000
2026 (to date)00000

What to do if you have a recalled Smisson-Cartledge Biomedical, LLC product

  1. Match the model, catalog or lot number on your device to the recall.
  2. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
  3. Report problems to FDA MedWatch.

See this week’s new recalls.

All Smisson-Cartledge Biomedical, LLC recalls

1 shown

Smisson-Cartledge Biomedical, LLC recall questions

How many recalls has Smisson-Cartledge Biomedical, LLC had?

3 recalls from Smisson-Cartledge Biomedical, LLC are on record with U.S. safety agencies, from 2021.

What is the most recent Smisson-Cartledge Biomedical, LLC recall?

Smisson-Cartledge Biomedical, LLC recalls ThermaCor 1200 Disposable Sets Components of the Smisson-Cartledge Biomedical ThermaCor 1200 Rapid Thermal Infusion, dated Feb 18, 2021. Every Smisson-Cartledge Biomedical, LLC recall is listed on this page, newest first.

What should I do if I have a recalled Smisson-Cartledge Biomedical, LLC product?

Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.

How do I get alerts for new Smisson-Cartledge Biomedical, LLC recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.