Every recall we track for Dutch Ophthalmic USA, Inc. — 3 in all — plus the complaints and injury reports the public filed about them.
Dutch Ophthalmic USA recalls Illuminated Stepped Laser Probe (Product Code 7510.ALC) due to barcode expiration date showing 2025 instead of 2024. This may cause confusion in product expiration tracking.
Dutch Ophthalmic USA recalls 23-gauge backflush brush needles labeled as 20-gauge. Mislabeled needles could cause surgical errors. Check product code 1281.B1D06 for affected items.
Dutch Ophthalmic USA recalls 25-gauge surgical packs containing 23-gauge infusion lines. This mismatch risks incorrect surgical use. Affected units have specific product numbers and lot codes.
