Medline Industries Recalls

4 recalls found for Medline Industries. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Medline recalls 14,379 Olympus biopsy valve kits over rubber fragments in 2026 recall

Medline Industries is recalling 14,379 bronchoscopy kits containing Olympus biopsy valves distributed nationwide in the United States. Olympus reports rubber fragments detaching from the valve slit, which could leave a foreign body in a patient’s tracheobronchial tree and may require removal. Hospitals should stop using the affected kits immediately and follow Medline’s recall instructions.

Medline Industries
Kits contain
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Health & Personal Care
HIGH
FDA DEVICE

Medline ENFIT G-Tube Connector ENFIT1010GC Recalled for Leakage Risk (651,789 Units, 2026)

Medline Industries recalled 651,789 ENFIT G-TUBE connectors (ENFIT1010GC) sold worldwide, including the United States and Canada. The connectors were not manufactured to required dimensional specifications and may not seal properly with ENFit-style devices, which could lead to leakage. Healthcare facilities and patients should stop using this device immediately and follow recall instructions from

Medline Industries
Connectors were
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Health & Personal Care
HIGH
FDA DRUG

Medline Recalls Povidone-Iodine Solution Due to Potency Issues

Medline Industries recalled 2,680 bottles of Povidone-Iodine 10% Solution on August 19, 2025. The product is subpotent, posing a risk to users. Consumers should stop use immediately and contact their healthcare provider.

POVIDONE-IODINE
Subpotent drug
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Brand Statistics

Total Recalls
4
Pages
1