Overview of recall records associated with Global Healthcare Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
The multi-sample needle retractable sheath may not fully retract over the needle during the changes of the blood collection tubes.
Firm was notified of a potential product defect related to kinking (flattening) of anesthesia extension tubes which may represent a potential health hazard.
This page summarizes recall records in which the official source identifies Global Healthcare 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.
