RC Outsourcing recalled 2,669 bevacizumab intravitreal syringes distributed nationwide to hospitals and clinics. The recall cites a lack of assurance of sterility. Stop using the product immediately and contact RC Outsourcing or your healthcare provider for guidance. Recall notices will be sent by letter.
Lack of assurance of sterility.
Consumers and healthcare providers should stop using this product immediately. Contact RC Outsourcing, LLC or your healthcare provider for guidance. Notification method: Letter
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Bevacizumab intravitreal injections are used to treat retinal diseases in adults and are prepared for hospital or office use. They are administered by ophthalmologists in a clinical setting.
A lack of sterility can result in contamination and eye infections, including serious conditions like endophthalmitis, requiring medical care.
This recall is not part of a broader industry pattern.
Hospitals and clinics must review stock, pause administrations, and coordinate with suppliers. The recall involves 2,669 syringes distributed nationwide, potentially affecting patient care workflows and budgets.
FDA enforcement page for D-0003-2026 and recall notices: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=D-0003-2026
Recall processing timelines vary; follow RC Outsourcing guidance. Typical recall-related refunds or replacements, when offered, can take several weeks
Retain all recall notices, packaging photos, lot numbers, communication with RC Outsourcing LLC, and records of stock disposition.
Bevacizumab intravitreal syringe, 0.25 mL total volume (1.75 mg/0.07 mL). Lot numbers being recalled: 20250708-768A26, 20250715-944DF2, 20250722-55C603, 20250722-5DC113. Sold to hospitals and clinics nationwide in the United States. Recall date: 2025-09-22. Quantity: 2,669 syringes. Price: Unknown.
No injuries or incidents have been reported.
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