创建报告

请提供报告标题

请提供位置

将我的报告设为私密

请提供详细信息

警报调节器提醒企业或产品所有者获取针对我的问题的通知

获取有关您案例的警报和更新！

这些信息不会显示在网站上。我们可以通知您更新，并可能与您联系以获取更多信息，以帮助您解决或跟进您的问题。

电子邮件

请提供电子邮件或电话

电话号码

请提供电子邮件或电话

在主页上显示我的报告

我们不会显示您的电子邮件或联系信息

跳过此步骤

我同意条款与条件

请接受我们的条款和条件

报告的电子邮件或短信副本

在下面输入以获取您的报告副本的电子邮件，或短信指向您的报告的链接

电子邮件

请提供电子邮件或电话

电话号码

请提供电子邮件或电话

我同意条款与条件

请接受我们的条款和条件

报告人

Message us

Cross Contamination

已更新: 2021年1月13日中午 12点00分

Covid-19 OSHA 投诉, Covid Testing Site - Indiana National Guard, 3380 S Walnut St, Bloomington, IN 47401, USA

3年前

交叉污染个人防护装备未经训练的员工没有正确佩戴拭子食品和饮料。

来源：osha.gov | 收据日期：2020-11-19

#coronaviruscovid19 #osha #crosscontamination #southwalnutstreet #bloomington #indiana #us

108

有帮助
跟随
添加报告
分享
- 复制链接

Fresenius Kabi USA Dexmedetomidine HCL 在 0.9％氯化钠注射液中-由于与利多卡因交叉污染而召回, USA

3年前 •source www.fda.gov

Recall notice

Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi USA
Product recalled: Dexmedetomidine HCL in 0.9% Sodium Chloride Injection
Reason of the recall: Cross Contamination with Lidocaine
FDA Recall date: November 19, 2020
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Dexmedetomidine HCl … 查看更多

in 0.9% Sodium Chloride Injection, 200 mcg/50 mL (4 mcg /mL), 50 mL fill in a 50 mL vial. Fresenius Kabi initiated this recall due to a trace amount of lidocaine present in the lot. This recall is being performed to the user level. To date, no adverse drug experience reports have been received for the recalled lot. Administration of Dexmedetomidine HCl containing trace amounts of lidocaine to a patient with lidocaine allergy could result in a potentially life-threatening allergic reaction.

Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection is approved for intravenous use and indicated for sedation of non-intubated patients prior to and/or during surgical and other procedures. Listed below is a table of the recalled lot distributed nationwide to wholesalers, distributors, hospitals and pharmacies between April 9, 2020 and April 13, 2020. An image of the label is also included below.

- Dexmedetomidine HCl in 0.9%. Sodium Chloride Injection, 200 mcg / 50 mL (4 mcg / mL), 50 mL fill in a 50 mL vial. NDC Number: 63323-671-50. Product Code: 671050. Batch number: 6123925. Expiration Date: 03/2022. First Ship Date: 04/09/2020. Last Ship Date: 04/13/2020

Fresenius Kabi is notifying its distributors and customers by letter and asking them to check their stock immediately and to quarantine and discontinue the use and distribution of any affected product.

Distributors should notify their customers and direct them to quarantine and discontinue distributing or dispensing any affected lots, and to return the product to Fresenius Kabi.

Customers with questions regarding this recall may contact Fresenius Kabi at 1-866-716-2459 Monday through Friday, during the hours of 8:00 a.m. to 5:00 p.m. Central Time. Consumers should contact their physician or health care provider if they have experienced any problems that may be related to taking or using this drug product.

Check the full recall details on www.fda.gov

Source: FDA

#drugs #recall #crosscontamination #us

Fresenius Kabi USA Dexmedetomidine HCL in 0.9% Sodium Chloride Injection - recalled due to cross contamination with Lidocaine 照片 #1

303

有帮助
跟随
添加报告
分享
- 复制链接

诈骗/欺诈-Info @dtasg. com, Wendell, North Carolina, USA

1周前 •reported by user-dtwnd318

我从这家公司订购了草坪椅买二送二。我支付了订单，但到目前为止还没有收到商品，我访问了网站。他们说他们会把追踪号码发给我，就像他们在收到并查看追踪编码时所做的那样，我看到这件商品在中国流通了一段时间，然后自动出现在北卡罗来纳州的罗利，上面写着已送达，我什么也没收到。订单号是 3***，这些人需要被拦住，因为我刚刚读到了另一份投诉，该投诉完全是我所说的逐字记录。

网站信息 @dtasga。com

#scam #onlineshopping #onlinescam #delivery #wendell #northcarolina #us