FDA 召回执法报告 D-0025-2027:Carolina Infusion 的 Tri-MIX 复方注射剂因无菌保证不足被列为 Class II 召回
FDA drug enforcement D-0025-2027: Carolina Infusion, LLC — Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
openFDA 药品召回执法报告 D-0025-2027 显示,Carolina Infusion 于 2026 年 9 月 10 日自主发起 Tri-MIX(PAPAV/PHENTO/ALPROS,30/1/60)复方注射剂召回,原因为加工设备导致无菌保证不足。
该执法报告记录了一起复方注射剂因加工设备导致无菌保证不足的召回分级、批号与效期信息,可供核对召回范围与分类依据。
FDA drug recall enforcement report — D-0025-2027
Report issued: 2026-10-14. This is the enforcement report date, not the recall initiation date.
Scope: one classified drug product recall record; event_id may group multiple products. Unclassified records without recall numbers are outside this stream. This record is not a press release or a new enforcement finding.
The openFDA dataset is updated weekly. Report status is not a live recall status and must not be used to track the recall lifecycle. Other dates below retain their named meanings.
Complete official product record (including openFDA harmonized identifiers):
{
"address_1": "95 Bees Creek Rd",
"address_2": "N/A",
"center_classification_date": "20261008",
"city": "Ridgeland",
"classification": "Class II",
"code_info": "Lot:08062026@10, BUD: 9/20/2026.",
"country": "United States",
"distribution_pattern": "Nationwide within the U.S",
"event_id": "99867",
"initial_firm_notification": "E-Mail",
"openfda": {},
"postal_code": "29936-7540",
"product_description": "Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/60, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936",
"product_quantity": "5 mL in patient specific syringe dose",
"product_type": "Drugs",
"reason_for_recall": "Lack of Assurance of Sterility: Related to processing equipment used in compounded product.",
"recall_initiation_date": "20260910",
"recall_number": "D-0025-2027",
"recalling_firm": "Carolina Infusion, LLC",
"report_date": "20261014",
"state": "SC",
"status": "Ongoing",
"voluntary_mandated": "Voluntary: Firm initiated"
}
来源:openFDA 已分级药品召回执法报告 · api.fda.gov