Material CVI2960, PICC LINE TRAY ,CENTURION PICC LINE TRAY, REORDER CVI2960, STERILE..., LATEX FREE, STERILE, CENTURION
FDA device recall Z-2304-2011 · posted 2011-05-27 · Terminated
Recall details
- Recalling firm
- Centurion Medical Products Corporation
- Reason for recall
- This voluntary sub-recall was initiated because the vials of Bacteriostatic Sodium Chloride Injection, USP, 0.9% utilized to make the products may contain visible particulates.
- Action taken
- Centurion Medical Products Corporation issued press on April 1, 2011, and sent an Urgent Voluntary Recall letter dated March 15, 2011, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to discontinue use of the kits immediately and instructions were provided for the return of the kits. Customers were also asked to complete a form to fax or email back to the firm regarding the number of kits the firm has in their possession. Customers were instructed to provide recall notification to other firm's who received the recalled kits from their direct account. For any questions regarding this recall call 631-924-4000, ext 142.
- Root cause
- Material/Component Contamination
- Status
- Terminated
- Product code
- LRS
- Quantity affected
- 390
- Distribution
- Nationwide Distribution
- Date initiated
- 2011-03-31
- Date posted
- 2011-05-27
- Date terminated
- 2011-09-13
- Location
- Williamston, MI
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