Medline procedure kits labeled as: 1) SHORT TERM INFUSAPORT ACCESS KIT, Reorder number DYNDC3188; surgery tray
FDA device recall Z-1041-2025 · posted 2025-01-28 · Open, Classified
Recall details
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Reason for recall
- Certain Medline kits were manufactured and distributed with Procedure Masks with SO SOFT Earloops, and SOFT TOUCH II Surgical Masks which were subsequently recalled for not meeting the bioburden testing requirements of EN 14683.
- Action taken
- Medline issued a MEDICAL DEVICE RECALL notice to its consignees on 11/18/2024 via USPS and email. The notice explained the reason for the recall and requested quarantine of affected products pending correction. The firm requested the completion of the response form, which upon receipt, Medline will send labels to affix to the affected products with the instructions for the consignee to remove the affected component prior to using the kit.
- Root cause
- Under Investigation by firm
- Status
- Open, Classified
- Product code
- LRP
- Quantity affected
- 1450 units
- Distribution
- US Nationwide distribution.
- Date initiated
- 2024-11-18
- Date posted
- 2025-01-28
- Location
- Northfield, IL
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