United States
Company name: J. M. Smucker CompanyBrand name: Natural Balance
Product recalled: Ultra Premium Chicken & Liver Paté Formula
Reason of the recall: Due to elevated levels of choline chloride
FDA Recall date: July 03, 2020
Recall details: The J. M. Smucker Company today announced a voluntary recall of one lot of Natural Balance® Ultra Premium Chicken & Liver Paté Formula canned cat food due to health concerns likely associated with elevated levels of choline chloride. Ingesting impacted product may cause nausea with excessive salivation, constricted pupils and poor vision, diarrhea or vomiting to more severe symptoms including difficulty walking, muscle shaking, tremors, irregular heartbeat, difficulty breathing, possible cardiac or respiratory failure and, in extreme situations, death. Pet parents are encouraged to contact their cat’s veterinarian immediately if their cat is displaying any of these symptoms.
If pet parents have any product matching the following description in their possession, they should stop feeding it to their cats and dispose of the product. This information can be found on the bottom of each can.
- Natural Balance® Ultra Premium Chicken & Liver Paté Formula canned cat food (5.5 oz). UPC: 2363353227. Lot code: 9217803. Best by: 08 04 2021
These products are most commonly sold in pet specialty retailers and online throughout the United States and Canada. No other Natural Balance® products are impacted by this recall.
The Company has received reports of adverse reactions. Pet parents that have questions or would like to report adverse reactions should call 888-569-6828, Monday through Friday, 8 a.m. – 5 p.m. ET or email anytime at info@naturalbalanceinc.com.
Check the full recall details on www.fda.gov
Source: FDA
最近有趣的报告
诈骗警报, Paola, Province of Cosenza, Italy
4天前 •reported by user-cbvz9717
我正在举报一个未订购的包裹, Yucca Avenue, Lancaster, CA, USA
2周前 •reported by user-xzxrw962
未订购的包裹, Bridgeport, CT, USA
1天前 •reported by user-yrhww433
Foveth 还以为是 judy 的蓝色牛仔裤, Foveth
1周前 •reported by user-zfkjc166
风险声明:服用每日最大剂量为2克的盐酸万古霉素口服溶液的成年患者USP 250 mg/5mL,由于瓶装过满,每天最多可服用4克的口服万古霉素。一些患有肠粘膜炎性疾病的患者也可能对万古霉素有显著的全身吸收。这些患者可能有发生与更高剂量万古霉素口服溶液相关的不良反应的风险。肾功能恶化可能与电解质异常(例如高钾导致心脏骤停)有关。
该产品的推荐最大日剂量允许量为2gm/天,并且处方500 mg/10mL的给药方案的患者将超过该每日剂量,这可能对肾功能不全患者有害。该错误发生在制造的手动瓶装阶段。
盐酸万古霉素口服溶液,USP,250mg/5mL,口服,用于治疗由金黄色葡萄球菌(包括耐甲氧西林菌株)引起的小肠结肠炎和由艰难梭菌引起的抗生素相关假膜性结肠炎。
用于口服溶液的盐酸万古霉素,USP,250 mg/5mL 受召回,由产品上注明的 NDC 编号标识 标签。本次召回中包括以下用于口服溶液的盐酸万古霉素的批号,USP,250 mg/5mL。
口服溶液用盐酸万古霉素,美国药典,250mg/5mL。
-包装尺寸:80 mL,有效期:2025 年 9 月,批号:22613003A,NDC 编号:69238-2261-3。
-包装尺寸:150 mL,有效期:2025 年 9 月,批次:22613004A,NDC 编号:69238-2261-7。
-包装尺寸:150 mL,有效期:2025 …
-包装尺寸:300 mL,有效期:2025 年 9 月,批号:22613005B,NDC 编号:69238-2261-5。
任何拥有被召回产品库存的人都应检查产品并立即隔离任何召回的批次。有盐酸万古霉素口服溶液(USP,250 mg/5mL,正在召回)的零售商应检查库存并停止分发任何受影响的批次。
如果您受到该产品的伤害,请务必举报。它可以帮助检测和解决问题,防止他人受到伤害,还可以进行更好的监控。如果症状持续存在,请就医。
公司名称:Amneal Pharmicals, LLC
品牌名称:Amneal
产品召回:用于口服溶液的盐酸万古霉素,USP,250 mg/5mL
召回原因:由于瓶子装得过满,效果超强
美国食品药品管理局召回日期:2024 年 3 月 27 日
来源:www.fda.gov
我收到了一个我没有订购的包裹, South Wolcott Avenue, Chicago, IL 60609, USA
1周前 •reported by user-nmkrw681
我收到了一瓶 subgenix bioribrose,我没订购, Columbia, SC, USA
1周前 •reported by user-zmxc7992
骗局, Halle (Saale), Germany
2周前 •reported by user-hkxtw484
报告人
重要-您的报告已排队-您的报告可能需要长达 12 小时才能显示在我们的主页上(如果未选择为私人)
访问我们的学习页面了解更多有用的信息,或者发送电子邮件给我们: support@safelyhq.com