Medline Convenience Kits: 1) DENTAL PACK, Model Number: DYNDA3003
Pending LLM rewrite. Source: FDA_DEVICE Z-1393-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
The recalled product
- Product
- Medline Convenience Kits: 1) DENTAL PACK, Model Number: DYNDA3003
- Manufacturer
- Medline Industries, LP
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- 1) DYNDA3003
- UDI-DI: 10195327257484(each)
- 40195327257485(case)
- Lot Number: 24EMC989
- 2) DYNDA3003
- Lot Number: 24CMF059A
- 3) DYNDA3003
- Lot Number: 24CMF059
- 4) DYNDA3003
- Lot Number: 24BBH600
- 5) DYNDA3003
- Lot Number: 23JBH393
- 6) DYNDA3003
- Lot Number: 23GBA134
- 7) DYNDA3003
- Lot Number: 23CBV199
- 8) DYNDA3003
- Lot Number: 23CBT510
- 9) DYNDA3003
- Lot Number: 23CBN951
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- HighMedtronic DLP One-Piece Pediatric Arterial Cannula Recalled for Foreign Material
FDA (Devices) · 2026-07-22
- HighVasoview Hemopro 2 Endoscopic Vessel Harvesting System Recall
FDA (Devices) · 2026-07-22
- SevereT-Lok Bone Marrow Tray Kits Recalled for Sterility Testing Failure
FDA (Devices) · 2026-07-22
- SevereMedtronic Bio-Medicus Adult Cannula Kit Recalled for Foreign Material
FDA (Devices) · 2026-07-22
- SevereAbiomed Impella CP Smart Assist Set Heart Pump Introducer Sheath Leakage
FDA (Devices) · 2026-07-22