ZOLL Circulation Zoll, REF 8700-000869-40, Cool Line (Heparin) IVTM Disposable Pack and recall — FDA Z-0063-2022
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Overview of recall records associated with ZOLL Circulation, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 29, Class I: 1.
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
Labeling update concerning potential leaks from the catheter or the start-up kit (SUK) tubing
This page summarizes recall records in which the official source identifies ZOLL Circulation, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.