Named by the State Drug Administration: Johnson & Johnson, Philips, Stryker...

Medical Network, July 6 hearing recently, the State Food and Drug Administration notified 5 cases of device recall problem products, 1 case is a secondary recall, the recall problem is shown in the yellow background
.

Ethicon Endoscopic Surgical Instruments Co.
, Ltd.

recalls linear cutting staplers and adjustable staple cartridges
Johnson & Johnson (Shanghai) Medical Equipment Co.
, Ltd.
reported that due to specific models and batches of products, there are linear cutting staples and staples in the package Incompatibility of the cartridges, the manufacturer Ethicon Endo-Surgery, LLC, has made the linear cutting stapler and the adjustable staple cartridge Linear Cutter 55/75mm and Selectable Cartridge/reloads (Registration Certificate No.
: National Mechanical injection into 20152020243) voluntarily recalled
.
The recall level is three
.

Philips Medical Systems Netherlands Co.
, Ltd.

recalled X -ray computed tomography equipment
Philips (China) Investment Co.
, Ltd.
reported that due to specific models and specific batches of products, when the patient’s weight unit is set to pounds, SynchroRight P3T (personalized patient Agreement) The software will increase the issue of contrast dose.
Philips Medical Systems Nederland BV, the manufacturer of Philips Medical Systems Nederland BV, has used the X-ray computerized tomography equipment Computed Tomography System (Registration Number: National Machinery Injection 20153060422, China National Machinery Injection 20173302330 , National Machinery Injection 20163061984) voluntarily recalled
.
The recall level is three
.

Stryker Medical recalls medical electric hospital beds
Stryker (Beijing) Medical DevicesCo.
, Ltd.
reported that because the recalled products are applicable to clinical institutions and not suitable for personal use in the home environment, this recall involves countries selling products to individual users, which are beyond the scope of application.
Stryker Medical Stryker Medical has voluntarily recalled medical equipment such as Electrical Hospital Beds (see the attachment for the registration certificate or filing certificate)
.
The recall level is three
.

　　Philips Medical Systems (Cleveland) Co.
, Ltd.

　　recalls positron emission and X -ray computed tomography systems
Philips (China) Investment Co.
, Ltd.
reported that due to specific models and batches of products, there is severe wear and tear of the monitor bracket assembly shaft Failure to identify may cause the monitor bracket assembly to fall off the suspension arm.
The manufacturer Philips Medical Systems (Cleveland), Inc.
Philips Medical Systems (Cleveland) Co.
, Ltd.
performs positron emission and X-ray computed tomography The system PET/CT Imaging System (registration number: National Machinery Injection 20143305863, China National Machinery Injection 20173301760, China National Machinery Injection 20183060453) was actively recalled
.
The recall level is three
.

　　Nobel Biocare AB’s secondary recall of dental ceramics Nobel Biocare
(Shanghai) Co.
, Ltd.
reported that due to specific models and specific batches of products, there was a problem that a sintering furnace used for production in March 2021 did not meet the appropriate sintering curve.
Nobel Biocare AB voluntarily recalled Nobel Procera Dental Ceramics (registration number: National Machinery Injection 20162635088)
.
The recall level is level two
.