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U.S. Department of Health and Human Services

Class 2 Device Recall Centurion

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 Class 2 Device Recall Centurionsee related information
Date Initiated by FirmApril 08, 2024
Date PostedAugust 28, 2024
Recall Status1 Open3, Classified
Recall NumberZ-2766-2024
Recall Event ID 94585
Product Classification Ear, nose, and throat surgical tray - Product Code OGR
ProductCenturion procedure kits labeled as: 1) BIOPSY KIT, Pack Number DYNDA1466A; 2) BIOPSY SKIN/LACERATION TRAY, Pack Number SUT20455; 3) CHEST TUBE INSERTION TRAY, Pack Number CHT560; 4) CUSTOM BIOPSY TRAY, Pack Number MNS4815; 5) PERITONSILLAR ABSCESS TRAY, Pack Number MNS3560; 6) PRE POST DIALYSIS, Pack Number DYNDC3274; 7) STEREO PROCEDURE TRAY, Pack Number DYNDC2859A
Code Information DYNDA1466A, Lot Number 2022040190; SUT20455, Lot Number 2022040190; CHT560, Lot Number 2021092290; MNS4815, Lot Number 2022040190; MNS3560, Lot Number 2021021790; MNS3560, Lot Number 2021092290; MNS3560, Lot Number 2021092890; MNS3560, Lot Number 2022040190; MNS3560, Lot Number 2022071490; MNS3560, Lot Number 2023121290; DYNDC3274, Lot Number 2023121290; DYNDC2859A, Lot Number 2021092290
Recalling Firm/
Manufacturer		 MEDLINE INDUSTRIES, LP - Northfield
3 Lakes Dr
Northfield IL 60093-2753
For Additional Information ContactKarin Johnson
886-359-1704
Manufacturer Reason
for Recall		Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
FDA Determined
Cause 2		Under Investigation by firm
ActionMedline Industries LP issued a recall notice to its consignees on 04/08/2024 via letter delivered via USPS and email. The notice explained the issue, provided a link to for information pertaining to the risk involved https://www.fda.gov/medical-devices/safety-communications/update-evaluating-plastic-syringes-made-china-potential-device-failures-fda-safety-communication) and request that the syringes within the convenience be discarded, except for circumstances where no alternative syringes are readily available. If these syringes must be used, closely monitor for leaks, breakage, and any other problems, and report any quality issues to Medline and the FDA. Distributors were directed to notify their customers. The firm issued a second recall notice (an expansion) on 05/02/2024 using the same methods.
Distributionworldwide
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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