Recalls / —
—#161482
Product
AVID TruCustom CATH PACK convenience kits, Item Code: LGHM036-14
- FDA product code
- LRO — General Surgery Tray
- Device class
- Class 2
- Medical specialty
- General, Plastic Surgery
- Affected lot / code info
- Lot, Expiration Date: 1190449, 2/1/2019; 1210124, 6/1/2019; 1217082, 8/1/2019; 1219275, 3/1/2019; 1221265, 3/31/2019; 1222551, 7/1/2019
Why it was recalled
Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
Root cause (FDA determination)
Nonconforming Material/Component
Action the firm took
An email notification was sent to all sales representatives with the BD recall notification and the following instructions: " Examine inventory for the affected AVID catalog numbers and lots noted in the Where Used Chart. If affected product is found: (1) discontinue use and quarantine impacted product immediately; and (2) promptly apply a recall label to each affected lot found. Once labeled with the recall label, product may be taken out of quarantine and made available for use. " All other components in the MAI/ AVID tray are unaffected by this recall and may safely be used. Labels may be printed using the label template attached. Or, upon receiving the following information I will be happy to overnight the required labels. Any revisions or alterations to the labels are prohibited. " Label Quantity- 1 for each affected tray, plus 1 for each outside carton. " Contact Name " Address " Phone Number Sales representatives were asked to confirm to QualityAssurance@owens-minor.com that your customers were notified.
Recalling firm
- Firm
- Avid Medical, Inc.
- Address
- 9000 Westmont Dr, Toano, Virginia 23168-9351
Distribution
- Distribution pattern
- Distributed in 10 states: IL, KY, LA, MA, MO, NY, OH, TX, VA, WI.
Timeline
- Recall initiated
- 2017-06-22
- Terminated
- 2018-10-12
- Status
- —
Source: openFDA Device Recall endpoint. Recall record ID #161482. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.