Medline FETOSCOPY CDS-LF Kits Recalled for Adhesive Removal Issues
Medline Industries is recalling 10 FETOSCOPY CDS-LF medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The source reports that the product is difficult to remove and leaves adhesive residue on the skin, but does not report any illnesses, injuries, or deaths.
Plain-English summary
Medline Industries, LP is recalling 10 units of MEDLINE medical convenience kits labeled as FETOSCOPY CDS-LF, Product Number/SKU CDS840215P. The recall is due to reports that the product is difficult to remove from patients and leaves adhesive residue on the patient's skin.
The affected kits were distributed worldwide, including the United States, Canada, Turkey, Australia, and the United Arab Emirates. The specific lot number is CDS840215P, with UDI/DI 10198459142031 for each unit and 40198459142032 for the case.
Healthcare facilities and consumers should stop using the affected kits and contact Medline Industries for further instructions or a return.
The recalled product
- Product
- MEDLINE medical convenience kits labeled as: FETOSCOPY CDS-LF, Medline Product Number/SKU CDS840215P
- Manufacturer
- Medline Industries, LP
- Affected units
- 10
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 (2)
- UDI/DI 10198459142031 (each) 40198459142032 (case)
- Lot numbers: CDS840215P
Distribution
Distributed nationwide across the United States.
Related recalls
Same manufacturer · Medline Industries, LP
See all →- ModerateMedline recalls medical convenience kits due to removal difficulty and skin residue
FDA (Devices) · 2026-10-28
- ModerateMedline C-Section Tray Kits Recalled for Adhesive Removal Issues
FDA (Devices) · 2026-10-28
- ModerateMedline Drape C-SEC Fen Clear Screen Wire Recall
FDA (Devices) · 2026-10-28
- ModerateMedline Recalls Hip Scope Packs Due to Removal Difficulties
FDA (Devices) · 2026-10-28
- ModerateMedline Medical Convenience Kits Recalled for Adhesive Removal Issues
FDA (Devices) · 2026-10-28
Same hazard · adhesive residue
See all →- ModerateMedline Medical Convenience Kits Recalled for Adhesive Removal Issues
FDA (Devices) · 2026-10-28
- ModerateMedline Tubal Ligation Kits Recalled for Adhesive Removal Issues
FDA (Devices) · 2026-10-28