NuVasive Specialized Orthopedics, Inc. recalls NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product Description:…
The Instructions for Use have been updated to include: (1) Clarification that the device is intended for use only in patients 18 years and older, (2) That patients should weigh 50 lbs. or more while undergoing…
Read the official notice →- Date
- 2021-12-08
- Country
- United States
- Brand
- NuVasive Specialized Orthopedics
- Product
- NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product Description: CPA1-000…
- Classification
- Class II
- Units
- U.S.: AK, AL, AR, AZ, CA, CO, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
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FDA · DeviceNuVasive Specialized Orthopedics, Inc.U.S distribution to states of: FL and NV.Official notice →- 2022-12-21
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NuVasive Specialized Orthopedics, Inc. recalls NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used to brace the spine during growth to minimize the progression of…
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FDA · DeviceNuVasive Specialized Orthopedics, Inc.Distribution US nationwide including Puerto Rico; Chile, Israel, Jordan, New…Official notice → - 2022-02-02
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Safety Alert to all surgeons informing them of post-implantation fractures of an internal metallic component for device manufactured prior to March 26, 2015.
Other drugs & medical recalls in the United States
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Wright Medical Technology Inc recalls INBONE Total Ankle System, INBONE POLY INSERT SZ 2+ 14mm SULCUS
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FDA · DeviceWright Medical Technology IncUS Nationwide distribution in the states of MI and PA.Official notice →