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openFDA 已分级药品召回执法报告·· 8 天前精选AI 评分77

FDA 药品执法报告 D-0855-2026:Sterling Pharmaceutical Services 因无菌保证不足召回羧甲基纤维素钠滴眼液

FDA drug enforcement D-0855-2026: Sterling Pharmaceutical Services LLC — Lack of Assurance of Sterility

AI 导读

openFDA 药品召回执法报告 D-0855-2026 显示,Sterling Pharmaceutical Services LLC 自愿召回 AvKare 羧甲基纤维素钠滴眼液 0.5%(15 mL 瓶装),原因为无菌保证不足,分级为 Class II。

推荐理由

该执法记录显示召回分级为 Class II,可帮助读者核对涉及的批号与全美分销范围。

正文 · AI 翻译

FDA 药品召回执法报告 — D-0855-2026

报告发布:2026-09-30。这是执法报告日期,不是召回启动日期。

范围:一条已分类的药品召回记录;event_id 可能归组多个产品。没有召回编号的未分类记录不在本数据流范围内。本记录不是新闻稿,也不是新的执法认定。

openFDA 数据集每周更新。报告状态不是实时召回状态,不得用于跟踪召回生命周期。以下其他日期保留其各自名称所对应的含义。

完整官方产品记录(包括 openFDA 统一标识符):

{

"address_1": "109 S 2nd St",

"address_2": "",

"center_classification_date": "20260921",

"city": "Dupo",

"classification": "Class II",

"code_info": "Lot# 3161, Exp 8/2026, Lot# 3245, Expiry: 3/2027; Lot# 3260, Expiry: 5/2027; Lot# 3298, Lot# 3299, and Lot# 3300, Expiry: 6/2027; Lot# 3301, Lot# 3302, Lot# 3305 and Lot# 3306, Expiry: 7/2027",

"country": "United States",

"distribution_pattern": "USA Nationwide",

"event_id": "99712",

"initial_firm_notification": "Letter",

"more_code_info": "",

"openfda": {

"application_number": [

"M018"

],

"brand_name": [

"CARBOXYMETHYLCELLULOSE SODIUM"

],

"generic_name": [

"CARBOXYMETHYLCELLULOSE SODIUM"

],

"is_original_packager": [

true

],

"manufacturer_name": [

"AvPAK"

],

"package_ndc": [

"50268-068-15",

"50268-068-02"

],

"product_ndc": [

"50268-068"

],

"product_type": [

"HUMAN OTC DRUG"

],

"route": [

"OPHTHALMIC"

],

"rxcui": [

"1188426"

],

"spl_id": [

"435361c6-ed83-3e7b-e063-6394a90ac92f"

],

"spl_set_id": [

"b479d2ae-4b59-916a-e053-2995a90af8ec"

],

"substance_name": [

"CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM"

],

"unii": [

"K679OBS311"

]

},

"postal_code": "62239-1351",

"product_description": "AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops, Sterile, 0.5 FL OZ (15 mL) bottle, Distributed by: AVKARE, Pulaski, TN, 38478, NDC 50268-068-15",

"product_quantity": "12,864 packs",

"product_type": "Drugs",

"reason_for_recall": "Lack of Assurance of Sterility",

"recall_initiation_date": "20260820",

"recall_number": "D-0855-2026",

"recalling_firm": "Sterling Pharmaceutical Services LLC",

"report_date": "20260930",

"state": "IL",

"status": "Ongoing",

"voluntary_mandated": "Voluntary: Firm initiated"

}

来源:openFDA 已分级药品召回执法报告 · api.fda.gov