Atlas FDA

V. Mueller Pfister-Schwartz Stone Retriever 4-Wire Basket, Without Filiform Tip; a sterile, single use kidney stone retr

FDA device recall Z-0179-05 · posted 2004-11-05 · Terminated

Recall details

Recalling firm
Cardinal Health
Reason for recall
The dispenser box was mislabeled with the wrong length and the wrong wire gauge.
Action taken
Field correction recall by letter dated 10/27/04, nforming the accounts of the mislabeling and providing corrective labels with the correct dimensions to place onto the dispensing box.
Root cause
Other
Status
Terminated
Product code
FFL
Quantity affected
32 units
Distribution
South Carolina, New York, Missouri, West Virginia, Texas and MIssissippi
Date initiated
2004-10-27
Date posted
2004-11-05
Date terminated
2004-12-21
Location
McGaw Park, IL

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