680,000 masks were urgently recalled.

July 2nd, the Department of Health and Social Security is recalling a number of masks that have been distributed to nursing homes and clinics, according to CCTV NewsIt is reported that the mask has expired for 7 years, some nursing home officials and doctors are very worried that health care workers and patients may be because of these outdated poor quality masks infected with the new crown viruson the same day, guangdong Drug Administration official website issued a recall information, Guangdong Zhaoyuan Industrial Co., Ltdreported that the company's production of disposable medical masks to implement an active recall processing, recall level of three, because the filtration did not meet the standardshas been hot lying around the topic of the quality of epidemic prevention materials such as masksRecently, Fujian, Chongqing, Jiangxi, Hubei and other places of the Drug Administration issued a series of mask recall notice, due to respiratory resistance, sterile, ear hanging short, basic size and other quality problems, a total of more than 680,000 masks were recalledinvolved Honeywell, Ruixin, Kanghua Weishi, Aiyi and other brands260,000 Honeywell KN95 masks were recalled due to poor filtration efficiency
, Xiamen Lisha Medical Technology Co., Ltdreported the recall plan to the Fujian Provincial Market Supervision Authority, will be recalled from now on, from January 8, 2019 to March 1, 2019 kn manufactured between January 8, 2019 95 self-absorbing filter anti-particle respirator (mask), model H1009101V/H910V, ear band with exhalation valve anti-counterfeiting particulate protection mask, involving a quantity of 261000 packs (1 /pack)the recallofed problem mask products:the scope of the recall KN95 self-absorbing filter anti-particulate respirator (mask), because the product non-oily particle filtration efficiency did not reach 95%, does not meet the national standard requirements, does not meet the expected filtering effect of KN95 mask, consumer protection safety does not play its due role in protection, there are certain safety risksXiamen Lisha Medical Technology Co., Ltdwill issue a recall plan in stores from May 15, 2020, prompting consumers holding the affected product stoates to stop using the product and contact Xiamen Lisha Medical Technology Co., Ltdor its distributors for free replacement, Fujian Huifeng Pharmaceutical Co , Ltd also issued a report, the product use of the minimum sales packaging label and product registration certificate content is not exactly consistent, the problem does not meet the relevant requirements, but will not have any impact on human use, has not received any complaints or adverse events arising from the problem, but in order to meet the standard requirements, the company research decision, the product does not meet the requirements of the recall, and correct the problem raw materials are not up to standard or lead to insufficient filtration efficiency, 17600 masks were recalled days ago, Chongqing Anti-Stack Machinery Co., Ltd in accordance with the requirements of the Interim Regulations on the Administration of Consumer Recalls, reported the recall plan to the Chongqing Municipal Market Supervision Administration, will be recalled from April 2020, the 175 x 95mm model saves, involving a total of 352 boxes (50 boxes), a total of 17,600 masks a one-time protective mask within the scope of this recall, there may be a safety hazard of insufficient filtration efficiency due to raw materials that do not meet the standard requirements For disposable protective masks within the scope of the recall, Chongqing Ampher Machinery Industry Co., Ltd prompts consumers holding the affected product stoopthement of the product to stop using the product and contacting Chongqing Ampher Machinery Industry Co., Ltd or its distributors for free replacement Jiangxi: 208,000 masks were recalled, of which 16,000 have been sold
recently, the State Drug Administration official website issued a number of notices that five enterprises have been actively recalled for the use of disposable masks, involving Nanchang Kanghua Weiwood Co., Ltd., Nanchang Xing Medical Devices Co., Ltd., Nanchang Yendley Medical Devices Co., Ltd., Jiangxi Aiyi Health Materials Co., Ltd., Jiangxi Jinhui Medical Devices Co., Ltd , the recall involves a total of 208,000 disposable masks, involving respiratory resistance, sterile, short ear hanging, basic size and other quality issues Of these, 16,000 have been destroyed, 16,000 have been sold and cannot be recalled, while the rest are now out of use and actively recalled as follows: Nanchang City Kanghua Weiwood Co., Ltd reported that, due to the one-time use of medical mask strapping, ventilation resistance, sterile does not meet the standard requirements, Nanchang City Kanghua Weiwood Co., Ltd for its production of disposable medical masks (registration certificate number: 20202140049) active recall, involving a total of 32,000, of which 16,000 sales can not be completed, another 16000 have been destroyed The recall level is Level 3 Nanchang Xingxing Medical Devices Co., Ltd reported that received customer reports, batch number 20200425 of the disposable medical mask off the ear band serious, Nanchang Xingxing Medical Devices Co., Ltd for its production of disposable medical masks (registration number: 20172640271) active recall The number of 80,000 has been discontinued with concurrent recall notices, with a level of three recalls Nanchang Yongdeli Medical Devices Co., Ltd reported that, because the basic size of disposable maskdoes not meet the standard requirements, Nanchang Yongdeli Medical Devices Co., Ltd for its production of disposable mask (registration certificate number: 20152640077) active recall The number of 1000 is involved and the recall level is level three Jiangxi Aiyi Health Materials Co., Ltd reported that due to the one-time use of mask ventilation resistance does not meet the standard requirements, Jiangxi Aiyi Health Materials Co., Ltd for its production of disposable mask (registration certificate number: 20152640189) active recall The number of 10,000 is involved and the recall level is level three Jiangxi Jinhui Medical Devices Co., Ltd reported that, because the basic size of disposable masks does not meet the standard requirements, Jiangxi Jinhui Medical Devices Co., Ltd for its production of disposable masks (registration certificate number: 20192140291) active recall The number of 85,000 is involved and the recall level is level three 4
ventilation resistance non-compliant Hubei: filtration efficiency, ventilation resistance is not up to standard, more than 200,000 masks were recalled
according to the Hubei Provincial Drug Administration official website issued in June, three enterprises to recall a total of 205899 disposable medical masks specifically, The Company of Jianghe Medical Materials Co., Ltd of Shenjiang City, because the supplier provided filter paper is not up to standard, resulting in the mask filtration efficiency is not qualified, so the recall of one-time medical mask7000 Wuhan Health Care Medical Technology Co., Ltd because of the product ventilation resistance index is high, recall editing 18899 disposable medical masks Xiantao Ruixin Protective Supplies Co , Ltd due to the sampling found that the mask bacteria filtration efficiency is not up to standard, the company produced 180,000 disposable medical masks (registration number: Egun injection 20166642249) for recall and destruction, recall level of three , the State Administration of Market Supervision and Administration issued the "Epidemic prevention materials product quality and market order special corrective action typical case." According to the official website disclosed, this rectification is in accordance with the Party Central Committee, the State Council decision-making deployment, requiring the local market regulatory departments to comprehensively check the quality of epidemic prevention materials and market order hidden dangers, comprehensive rectification of production, circulation, consumption of outstanding problems the rapid action of the local market regulatory authorities, continue to strengthen supervision, in accordance with the law strictly and strictly investigated a number of illegal cases, and effectively maintain the order of the epidemic prevention materials market On June 3, , the State Drug Administration convened a video dispatch meeting on the supervision and sampling of medical devices for epidemic prevention and control, and further implemented the National Action Plan for the Quality of Epidemic Prevention Materials and Market Order of the National Epidemic Prevention Materials Product Quality and Market Order, requiring relevant departments in all regions of the country to carry out corrective actions rectification is the whole process, will run through the production, circulation, consumption, export of epidemic prevention materials chain supervision The source of production, enterprise qualification, product standards, product quality will be checked at the same time, the whole process of non-conforming products will be traced back to the law to investigate the responsibility of production operators, strict inspection of the quality of export epidemic prevention materials.