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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Vitreq Bv: Microscopic tears of the sterile pouch may compromise sterility

Agency Publication Date: January 24, 2020
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Affected Products

Product: (1) VitreQ 23G BF Blunt Needles-BF23.D51 GTIN#: 8719214221126 (2) VitreQ 23G BF Brush Needles-BF23.D52 GTIN#: 8719214221140

All lots

Product: (1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2) VitreQ 25G BF Brush Needles-BF25.D52 GTIN: 8719214221188

All lots

Product: (1) VitreQ 20G BF Blunt Needles-Ref: BF20.D51 GTIN: 8719214221089 (2) VitreQ 20G BF Brush Needles-REF: BF20.D52 GTIN: 8719214221102

All lots

Product: VitreQ 23G PFC Injection Needle- Ref: MD23.D01 GTIN: 8719214221362

All lots

Product: VitreQ 25G PFC Injection Needle-Ref: MD25.D01 GTIN: 8719214221386

All lots

Product: VitreQ 23G VFI Cannula-REF: CN23.D03 GTIN: 8719214221423

All lots

Product: VitreQ 25G VFI Cannula-REF: CN25.D03 GTIN: 8719214221447

All lots

Product: VitreQ 27G VFI Cannula-REF: CN27.D03 GTIN: 8719214221461

All lots

Product: VitreQ 20G VFI Cannula-REF: CN20.D03 GTIN: 8719214221485

All lots

Product: VitreQ 23G Silicone Tipped Cannula-CN23.D01 GTIN: 8719214221508

All lots

Product: VitreQ 25G Silicone Tipped Cannula-REF: CN25.D01 GTIN: 8719214221522

All lots

Product: VitreQ 23G Pick Needles-REF: CN23.D04 GTIN: 8719214221584

All lots

Product: VitreQ 25G Pick Needles-REF: CN25.D04 GTIN: 8719214221607

All lots

Product: VitreQ 23G Blunt Needles with luer-lock connector-REF: CN23.D05 GTIN: 8719214221621

All lots

Product: VitreQ 25G Blunt Needles with luer-lock connector-REF : CN25.D05 GTIN: 8719214221645

All lots

Product: VitreQ 27G Blunt Needles with luer-lock connector-REF: CN27.D05 GTIN:8719214221669

All lots

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84661
Status: Resolved
Manufacturer: Vitreq Bv
Manufactured In: Netherlands

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.