Overview of recall records associated with Windstone Medical Packaging, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 28, Class I: 6.
Due to convenience kits containing a kit component that is under a recall action for improper use.
Due to convenience kits containing a kit component that is under a recall action for improper use.
Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an…
Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an…
Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an…
Due to Customer Convenience Kits containing 3M Steri-Drape Surgical Drapes that have been recalled by 3M Healthcare.
Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International, that are subject to a drug recall due to uncertainty of the…
Monoject 0.9% Sodium Chloride Flush Syringe Manufactured by Cardinal Health and placed into kits. Potential for the plunger to draw back after air has been expelled and reintroduce air back…
Angio tubing included within Custom Convenience kits may contain insufficient or incomplete weld
Angio tubing included within Custom Convenience kits may contain insufficient or incomplete weld
This page summarizes recall records in which the official source identifies Windstone Medical Packaging, 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.
