Recall Z-1173-2022— Busse Hospital Disposables, Inc.

Class II · Terminated

Class II FDA medical device recall by Busse Hospital Disposables, Inc., initiated 2022-02-22, terminated 2024-04-17. FDA's recall record names no specific 510(k) clearance for this event. Product: Pump Refill Kit Catalog Number: 7347R1. Reason: Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufacture the drug products.

Recalling firm
Busse Hospital Disposables, Inc.
Classification
Class II
Status
Terminated
Initiated
2022-02-22
Terminated
2024-04-17
Firm location
Hauppauge, NY, United States

Product description

Pump Refill Kit Catalog Number: 7347R1

Reason for recall

Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test methods used to manufacture the drug products

Data sourced from openFDA. This site is unofficial and independent of the FDA.