MicroPort Orthopedics Inc. recalls EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.
One confirmed incident has been received that EFSRN4PR, lot number MP1982170, Size 4 Evolution MP Non-Porous Femoral Right was opened during surgery and contained part number EFSRN3PL, lot number MP1982097, Size 3…
Read the official notice →- Date
- 2024-07-10
- Country
- United States
- Brand
- MicroPort Orthopedics
- Product
- EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.
- Classification
- Class II
- Units
- International distribution in the country of China. There is no field…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More MicroPort Orthopedics recalls
- 2026-01-28
USMicroPort Orthopedics Inc. recalls Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog Number: HTHT0036 Software Version: N/A Product…
Due to products not having FDA Premarket authorization to be distributed within the United States.
FDA · DeviceMicroPort Orthopedics Inc.The product was sent to distributors in multiple US states, including Texas,…Official notice →- 2024-12-25
- US
MicroPort Orthopedics Inc. recalls EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE…
Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packaging.
- 2023-02-22
- US
MicroPort Orthopedics Inc. recalls EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base
One confirmed incident has been received that ETPKN2PL lot 1916559, size 2 Evolution MP Tibial Base, was opened during surgery and contained ETPKN7SL lot 1916715, size 7 Evolution MP Tibial Base, in the packaging.
FDA · DeviceMicroPort Orthopedics Inc.International Distribution to countries of: Germany, Italy, France, Belgium,…Official notice → - 2022-06-08
- US
MicroPort Orthopedics Inc. recalls PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK
One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body.
FDA · DeviceMicroPort Orthopedics Inc.Worldwide distribution - US Nationwide distribution in the states of FL, IN,…Official notice →
Other drugs & medical recalls in the United States
- 2024-07-10
- US
Megadyne Medical Products, Inc. recalls Brand Name: MEGADYNE" MEGA SOFT" Reusable Patient Return Electrode Product Name: MEGADYNE" MEGA SOFT" Reusable Patient Return…
To limit the use of the Mega Soft Pads to patients aged 12 or older to mitigate the potential risk of patient burns identified with use of Mega Soft pads.
FDA · DeviceMegadyne Medical Products, Inc.Domestic: Nationwide distribution International: AUSTRALIA, AUSTRIA, BAHRAIN,…Official notice → - US
First Source Inc recalls First Source Vision M. Portable cart and platform that supports an X-ray system and laptop computer.
Potential for the bolt that secures the positioning arm to the gas spring to come loose and fall onto patient.
FDA · DeviceFirst Source IncWorldwide - US Nationwide distribution in the states of AR, CA, FL, GA, IL,…Official notice → - US
Ortho-Clinical Diagnostics, Inc. recalls VITROS Chemistry Products Calibrator Kit 29- In-Vitor used to calibrate the VITROS 5,1 FS/4600 Chemistry Systems and the VITROS…
Kit assigned an extended expiration date of 24-Jul-2025 during release. The correct expiration date for Lot 2953 is 24-Jul-2024. If used past its true expiration and the customer does not have their Assay Data Disk…
FDA · DeviceOrtho-Clinical Diagnostics, Inc.Worldwide distribution - US Nationwide including Puerto Rico and the countries…Official notice → - US
WOM World Of Medicine AG recalls WOM Tube Set for lrrlgatlon, single-use- Intended to transport irrigation fluid to the patient in endoscopic surgeries. Distr. by…
Incorrect transponder data was written on the RFID tags triggers the error message E03, Tube Set lnvalid, may result in a delay of surgery
- US
Siemens AG/Siemens Healthcare GmbH recalls ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional…
A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient…
FDA · DeviceSiemens AG/Siemens Healthcare GmbHWorldwide - US Nationwide distribution in the states of TX, MA, NH, MN, OK,…Official notice → - US
Philips North America Llc recalls Avalon Ultrasound Transducer. Directs low-energy ultrasound beam toward the fetal heart and externally monitors fetal heart rate.
Potential for inaccurate fetal heart rate measurements when monitoring multiples.
FDA · DevicePhilips North America LlcWorldwide distribution - US Nationwide and the countries of AD, AE, AR, AT,…Official notice →