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再见！ 和最良好的祝愿在你的恢复
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Covid-19 OSHA 投诉, Tesla, 901 Page Ave, Fremont, CA 94538, United States
Tesla, 901 Page Ave #7341, Fremont, CA 94538, USA
2020年11月25日 中午 12点00分
“'-担心座位部门新的 COVID 19 感染缺乏与员工沟通。T8 CCR 第 3203
来源：osha.gov | 收据日期：2020-06-09 少看”
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Covid-19 OSHA 投诉, UCSF Medical Center, 505 Parnassus Ave, San Francisco, CA 94143, USA
UCSF Medical Center, 505 Parnassus Ave, San Francisco, CA 94143, USA
2020年11月25日 中午 12点00分
“护士和医生休息室对于员工来说太小。没有提供物理距离区域。
据称危险：1，员工暴露：1
来源：osha.gov | 收据日期：2020-07-15 少看”
有帮助
Covid-19 OSHA 投诉, Target Distribution Center, 8940 East Rita Park Dr, Tucson, AZ 85747, USA
Target Distribution Center, 8940 East Rita Park Dr, Tucson, AZ 85747, USA
2020年11月25日 中午 12点00分
“1-所有员工使用的制冰机不会用消毒剂消毒或擦拭以防止 COVID-19 在工作场所的传播。2-雇主在工作时不强制使用口罩或面罩。3-断间的员工坐得更近 6 英尺管理层也意识到这种情况正在发生。4-人力资源部和领导层共同努力骚扰提出工作场所安全问题的员工。
涉嫌危险：4，员工暴露：60
来源：osha.gov | 收据日期：2020-10-07... 查看更多 少看”
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Covid-19 OSHA 投诉, United States Postal Service, 11151 Valley Blvd, El Monte, CA 91731, USA
United States Postal Service, 11151 Valley Blvd, El Monte, CA 91734, USA
2020年11月25日 中午 12点00分
“据报道，该设施的一名员工经检测 COVID-19 阳性。雇主没有进行接触者追踪和隔离与检测呈阳性的雇员接触的员工。员工可能暴露于 COVID-19。
来源：osha.gov | 收据日期：2020-10-29... 查看更多 少看”
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Covid-19 OSHA 投诉, Thunder Valley Casino Resort, 1200 Athens Ave, Lincoln, CA 95648, USA
Thunder Valley Casino Resort, 1200 Athens Avenue, Lincoln, 95648 California, United States
2020年11月25日 中午 12点00分
“1.由于缺乏个人防护设备，员工/经销商面临健康危害，例如经销商与公众互动时没有提供面罩等。员工/经销商面临健康危害，因为尚未针对与 COVID-19 相关的员工安全实施工程和行政控制（Plexiglas 隔板、洗手液、保持社交距离）。
来源：osha.gov | 收据日期：2020-07-01... 查看更多 少看”
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Covid-19 OSHA 投诉, Expedition Lodge, 168 N Main St, Moab, UT 84532, United States
Expedition Lodge, 168 N Main St, Moab, UT 84532, USA
2020年11月25日 中午 12点00分
“员工没有按照 COVID-19 的要求佩戴口罩。
据称危险：1，员工暴露：1
来源：osha.gov | 收据日期：2020-11-10 少看”
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Covid-19 OSHA 投诉, Real Athlete Academies, South 800 West, Pleasant Grove, UT 84062, USA
Real Athlete Academies, 844 S 800 W, Lindon, UT 84042, USA
2020年11月25日 中午 12点00分
“员工没有按照 COVID-19 的要求佩戴口罩
据称危险：1，员工暴露：1
来源：osha.gov | 收据日期：2020-11-10 少看”
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Covid-19 OSHA 投诉, Lowe's Home Improvement, Plaza Center Dr, West Jordan, UT 84084, United States
Lowe's Home Improvement, 7456 South, Plaza Center Dr, West Jordan, UT 84084, USA
2020年11月25日 中午 12点00分
“1.在花园中心没有口罩的员工。2.员工在结账时使用鼻子下面罩注册。
据称危险：2，员工暴露：2
来源：osha.gov | 收据日期：2020-11-09 少看”
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Covid-19 OSHA 投诉, Hoyt Archery, 593 N Wright Brothers Dr, Salt Lake City, UT 84116, USA
Hoyt Archery, 593 N Wright Brothers Dr, Salt Lake City, UT 84116, USA
2020年11月25日 中午 12点00分
“1.员工不戴口罩。2.员工用抹布擦嘴，然后使用同样的抹布擦拭设备。员工在共享设备上打喷嚏。
据称危险：3，员工暴露：10
来源：osha.gov | 收据日期：2020-11-09 少看”
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Covid-19 OSHA 投诉, Animal Emergency & Specialty Center, 17701 Cottonwood Drive, Parker, CO 80134, USA
Animal Emergency & Specialty Center, 17701 Cottonwood Dr, Parker, CO 80134, USA
2020年11月25日 中午 12点00分
“1.)员工可能会接触新型冠状病毒 COVID-19，原因包括：COVID-19 检测结果阳性后缺乏足够的隔离指南；每次轮班开始时缺乏温度筛查；普通表面清洁程序不足，包括但不限于到门把手、厨房区和浴室。违反 1970 年的《职业安全和健康法》，第 5 (a) (1) 节。由于施工期间的隔离措施不足，员工可能会暴露在二氧化硅粉中。员工接触干切和打磨含硅石膏板所产生的灰尘，而隔离措施不足以充分隔离危险材料。与 1910.1053 相反。3.)由于层压地板安装期间通风不足，员工可能会接触甲醛。员工暴露在不受控制的脱气甲醛蒸气中。与 1910.1048 相反。4.)员工可能暴露在工作场所施工所产生的危险... 查看更多噪音。与 1910.95 年相反。
涉嫌危险：5，员工暴露：50
来源：osha.gov | 收据日期：2020-10-17 少看”
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最近有趣的报告
Paroex 葡萄糖酸氯己定口服冲洗，4 盎司和 16 盎司-由于潜在污染 Burkholderia 而召回, USA
PDQ Restaurant, United States
2020年10月28日 上午 11点00分
“Company name: Sunstar Americas, Inc.
Brand name: Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: October 28, 2020
Recall details: Sunstar Americas, Inc. (SAI) is voluntarily... 查看更多recalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 6/30/22 – 9/30/22 (see specific lots below) to the consumer level. This product may be contaminated with the bacteria Burkholderia lata.
Use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such as pneumonia and bacteremia. To date, no adverse events have been reported to SAI related to this recall. The prescription oral rinse product, available through healthcare professionals only, is indicated for use as part of a professional program for the treatment of gingivitis and is packaged as follows:
- 1789P GUM® Paroex® is distributed in cases each containing 6 amber bottles of 16 fluid ounce (473 ml) chlorhexidine rinse. The bottle has a childproof cap and a 15 ml metered dosage cup, is safety sealed, and is decorated with a multiple-panel wrap-around label.
- 1788P GUM® Paroex® is distributed in cases each containing 24 amber bottles of 4 fluid ounce (118.25 ml) chlorhexidine rinse. The bottle has a childproof cap, is safety sealed, and is decorated with a multiple-panel wrap-around label.
The product can be identified by as shown in the images below: Paroex was distributed Nationwide to Dental offices, Dental distributors, Pharmaceutical wholesalers, Dental schools, and Pharmacies. SAI is notifying its direct distributors and customers by USPS Priority mail and is arranging for return of all recalled products. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.
Consumers with questions regarding this recall can contact SAI by phone at 1-800-528-8537 or email us.pcr@us.sunstar.com on Monday-Friday from 8am-5pm CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product. Affected products and lot numbers are detailed in the link below.
Check the full recall details on fda.gov
Source: FDA 少看”
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Lohxa Colhexidine 葡萄糖酸口服冲洗 USP，0.12％ 不含酒精-因为它可能被 Burkholderia lata 污染, USA
PDQ Restaurant, United States
2020年11月9日 下午 5点00分
“Company name: Lohxa, LLC
Brand name: Lohxa
Product recalled: Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free
Reason of the recall: May be contaminated with Burkholderia lata
FDA Recall date: November 09, 2020
Recall details: Lohxa, LLC is voluntarily recalling Chlorhexidine Gluconat... 查看更多e Oral Rinse USP, 0.12% Alcohol free (NDC:70166-027-15) products bearing an expiration date from 01/31/21 – 03/31/21 (see specific lots below) to the consumer level. This product is sourced and repackaged from Sunstar Americas Inc. who has notified us the product may be contaminated with the bacteria Burkholderia lata.
Use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such as pneumonia and bacteremia. To date, no adverse events have been reported to Lohxa, LLC related to this recall.
The prescription oral rinse product, available through institutional use only, is indicated for use as part of a professional program for the treatment of gingivitis and is packaged as follows:
- Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free is distributed in cases each containing 50 unit dose cups. Each case contains a colored label around the lid and body of the case.
The product can be identified by as shown in the images below. Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free was distributed to Nationwide to hospital pharmacies. Lohxa, LLC is notifying its direct customers by Fedex overnight mail, electronic mail, phone call and is arranging for return of all recalled products.
Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately. Consumers with questions regarding this recall can contact Lohxa, LLC by phone at 1-800-641-5564 or email info@lohxa.com on Monday-Friday from 8am-5pm EST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product. Affected products and lot numbers follow below:
- Chlorhexidine Gluconate Oral Rinse USP, 0.12% Alcohol free, 15 mL (NDC:70166-027-15) LOT/ EXP: T09101A/01/2021 |T08292A/02/2021 |T10011A/02/2021 |M10193A/03/2021 |T10223A/03/2021
Check the full recall details on fda.gov
Source: FDA 少看”
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CORE 必需营养素和免疫增强舌下维生素 D3-因未获批准的新药而召回, USA
PDQ Restaurant, United States
2020年11月23日 下午 2点00分
“Company name: Fusion Health and Vitality LLC
Brand name: CORE, Immune Boost
Product recalled: CORE essential nutrients and Immune Boost Sublingual Vitamin D3
Reason of the recall: Unapproved new drug
FDA Recall date: November 23, 2020
Recall details: Fusion Health and Vitality LLCis voluntaril... 查看更多y recalling all 2020 Lots of CORE essential nutrients and Immune Boost Sublingual Vitamin D3. CORE has been found to contain an unapproved food additive, hordenine HCl, rendering it adulterated. Immune Boost Labeling was found to contain statements that caused it to become and unapproved new drug under FDA labeling laws. Hordenine HCl is possibly unsafe when taken by mouth. Hordenine HCl might have similar stimulant effects and side effects such as rapid heart rate and high blood pressure.
Fusion Health and Vitality LLC has not received any reports of adverse events related to this recall. Please review the attached photos for identification. We began shipping Core Essential Nutrients on 1/2/2020 and we began shipping Immune Boost Sublingual Vitamin D3 on 4/15/2020. Both products are packaged with labels which prominently display the product name. CORE essential nutrients are found in a dark colored jar, in powdered format.
This product was formulated to mix into a liquid before consumption. The Immune Boost sublingual was packaged in a 2 ounce bottle that came with a sublingual application dropper. Fusion Health and Vitality is notifying its customers by email and is arranging for return of all recalled products. Consumers that have product which is being recalled should stop using it and return it to Fusion Health and Vitality for destruction. Consumers with questions regarding this recall or how to return recalled product can contact Fusion Health and Vitality by calling 1-888-964-5327, 9am to 5pm, Monday Thru Friday, EST. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
Source: FDA 少看”
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沃尔玛超级中心，马洛尼西部大道，加拿大 QC, Walmart Supercentre, Boulevard Maloney Ouest, Gatineau, QC, Canada
Walmart Supercentre, 640 Boulevard Maloney O, Gatineau, QC J8T 8K7, Canada
2020年11月15日 晚上 8点18分
“他们实际上迫使人们将洗手液放在手上，即使他们不需要这样做。我对其中一些东西过敏，因为我不知道他们手里有什么消毒剂，我的手都破裂和破裂。即使没有法律，他们实际上仍然迫使人们这样做。... 查看更多 少看”
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他们没有报告积极的 COVID 案例, In-N-Out Burger Distribution Center, Hamburger Lane, Baldwin Park, CA, USA
13502 Hamburger Ln, Baldwin Park, CA 91706, USA
2020年10月31日 凌晨 12点15分
“我是鲍德温公园的肉类部门的屠夫他们没有报告 COVID 的正面案例。他们刚刚开始社交距离。主管、管理人员和同事都是粗心的阳性或有症状。一个同事已经失去了他的妹妹，以粗心。他从来没有被隔离在 n 出汉堡是负责病毒在整个加利福尼亚州的传播很大一部分.... 查看更多 少看”
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3 人s 发现此评论有帮助
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
PDQ Restaurant, United States
2020年11月19日 晚上 6点01分
“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 singl... 查看更多e lot of Dexmedetomidine HCl 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 fda.gov
Source: FDA 少看”
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全食品市场通心粉和奶酪产品-由于未申报的鸡蛋召回, USA
Friendsville, MD 21531, USA
2020年10月28日 晚上 10点00分
“Company name: Whole Foods Market
Brand name: Whole Foods Market
Product recalled: Macaroni and Cheese products
Reason of the recall: Undeclared egg
FDA Recall date: October 28, 2020
Recall details: Whole Foods Market is voluntarily recalling select prepared Macaroni & Cheese products from store... 查看更多s across five states because they contain undeclared egg. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume these products.
The affected products were sold at Whole Foods Market stores in Maryland, New Jersey, Pennsylvania, Virginia and Washington, D.C. The product was sold in plastic containers and in family-style meal kits with Whole Foods Market scale labels in the prepared foods department, available both hot and refrigerated. The product was also available from the chef’s case counter and from Whole Foods Market online and catering menus. The affected products can be identified by the following information. All affected product has been removed from store shelves. No allergic reactions have been reported to date.
- Macaroni & Cheese, chef’s case. Product Code (begins with) M: 286501. Best by 10/28/2020
- Macaroni & Cheese, packaged. Product Code (begins with) M: 263608. Best by 10/27/2020
- Macaroni & Cheese, online and catering. Product Code (begins with) M: 114449 | 109866. Best by 10/23/2020
- Rotisserie Chicken Meals with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 261596 | 261580 | 261590 | 261601 | 261608 | 261616. Best by 10/26/2020
- Fried Chicken Meal with Mac & Cheese, packaged. Product Code (begins with) M: 247257. Best by 10/25/2020
- Fried Chicken Meal with Mac & Cheese, packaged on hot bar. Product Code (begins with) M: 237444. Best by 10/24/2020
- Chicken Rustico Romano Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 241442. Best by 10/28/2020
- Chicken Breast Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 299430. Best by 10/28/2020
- BBQ Turkey Meatballs Chef Plate with Mac & Cheese and Green Beans, packaged. Product Code (begins with) M: 241464. Best by 10/28/2020
- Roasted Turkey Chef Plate with Mac & Cheese and Broccoli, packaged. Product Code (begins with) M: 242019. Best by 10/28/2020
Customers who purchased this product at Whole Foods Market can bring a valid receipt into stores for a full refund. Consumers with additional questions can call 1-844-936-8255 between the hours of 7:00 a.m. and 10:00 p.m. CST, Monday through Friday, or 8:00 a.m. and 6:00 p.m. Saturday through Sunday.
Check the full recall details on fda.gov
Source: FDA 少看”
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Covid-19 OSHA 投诉, Kroger, 2010 Whittaker Rd, Ypsilanti, MI 48197, USA
Kroger, 2010 Whittaker Road, Ypsilanti, 48197 Michigan, United States
2020年11月10日 中午 12点00分
“1.雇主未能在门口检查口罩；顾客正在未蒙面或没有遮住鼻子的情况下进入。雇主未能检查和记录员工的温度。
来源：osha.gov | 收据日期：2020-09-14 少看”
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Covid-19 OSHA 投诉, JCPenney, 1100 N Wesleyan Blvd, Rocky Mount, NC 27804, USA
JCPenney, 1100 N Wesleyan Blvd, Rocky Mount, NC 27804, USA
2020年11月10日 中午 12点00分
“1.商店雇员中至少有三例 COVID-19 病例，雇主没有通知其他雇员，以便在他们与个人接触的情况下可以对他们进行测试。雇主没有在商店进行任何清洁或消毒。
来源：osha.gov | 收据日期：2020-10-07... 查看更多 少看”
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Covid-19 OSHA 投诉, Republic Services, 3150 N 7th St Trfy, Kansas City, KS 66115, USA
Republic Services, 3150 N 7th St Trfy, Kansas City, KS 66115, USA
2020年11月18日 中午 12点00分
“1.不提供坠落保护，员工必须共爬 13 英尺才能上卡车。1910.501 (a) [地点：维修店] 2.洗眼站已破坏管道，无法正常工作。1910.151 (c) [地点：主管办公室旁边的维修店] 3.雇主要求员工使用玻璃纤维中的 A 形梯子，而且在几个地方它们被破坏。1910.23 4.延长线和电动工具磨损并且接线暴露。1910.303 5.油继续从软管滴到地板上，没有固定并造成滑落危险; 一些零件/工具/垃圾遍布整个商店，造成跳闸危险。1910.22 6.一个出口门没有正确标记为非出口/出口 1910.37 7.过去 1.5 年没有举行安全会议 8.天花板/屋顶材料每天都落在员工身上，工具箱... 查看更多全天。[一般责任 5 (a) (1)] 9.灭火器没有每月检查一次。灭火器不在彼此之间适当距离的地方. 1910.157 10.液体瓶/桶没有正确标记; 安全数据表没有更新. 1910.1200 11.使用过的油和燃料过滤器正被丢弃在普通垃圾桶中，以及使用过的吸油剂；气溶胶罐被弃置在普通垃圾桶中，然后在商店中散布，而不是放在消防柜里。1910.120 12.雇主没有为防止 COVID-19 的传播而强制使用口罩 [一般责任 5 (a) (1)]
来源：osha.gov | 收据日期：2020-10-01 少看”
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