Blue Belt Technologies, Inc recalls CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S
Possibility that the user is unable to resolve drill disconnection error messages.
Read the official notice →- Date
- 2024-01-17
- Country
- United States
- Brand
- Blue Belt Technologies
- Product
- CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S
- Classification
- Class II
- Units
- Domestic: Nationwide Distribution.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Blue Belt Technologies recalls
- 2024-06-19
USBlue Belt Technologies, Inc recalls CORI Starter Kit, Real Intelligence CORI, CORI STARTER KIT - UNIVERSAL.Intended to assist the surgeon in providing software-defined…
CORI Surgical System with Real Intelligence Software exhibits an increased Marker Registration Error (MRE) which may cause tracker arrays to flicker on screen of the CORI Surgical System during use, and may cause…
FDA · DeviceBlue Belt Technologies, IncNationwide Foreign: Australia, Austria, Belgium, Brazil, Canada, Chile, China,…Official notice →- 2023-10-11
- US
Blue Belt Technologies, Inc recalls Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number: ROB10299
CORI software was missing a planning stage that appears in cases of significant knee deformation (outside of the range of 3 degrees valgus to 7 degrees varus) when the surgeon chooses to define the femoral rotational…
Other drugs & medical recalls in the United States
- 2024-01-17
- US
mo-Vis BVBA recalls Scoot Control R-net, Product Number P015-61. The Scoot Control is intended to support a wheelchair attendant in controlling or maneuvering…
In rare cases, the lever of the throttle can get temporarily stuck during the movement and does not come back to its neutral point by itself. If this happens during usage, an unwanted movement of the chair could be the…
- US
Ortho-Clinical Diagnostics, Inc. recalls QMS Tacrolimus Calibrators, Product code 10015573
Ortho-Clinical Diagnostics, Inc. is recalling QMS Tacrolimus Calibrators, Lot 74859619 expiry date: May 11, 2024, due to improper storage that is expected to degrade the quality of the calibrator and render it…
FDA · DeviceOrtho-Clinical Diagnostics, Inc.Domestic distribution to IL, IN, FL, NJ, NM, TX. International distribution to…Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Gown Poly W/Breath Sleeves XL AAMIK Level 4 (Eclipse gown), REF SPT-2208CS, 100/pack, Non-Sterile.
Surgical gowns were manufactured with the wrong sleeve.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldDistribution was made to MD, OH, TN, TX, and WI. There was no…Official notice → - US
Baxter Healthcare Corporation recalls XScribe CP Cardiac Stress Testing System, version 6, with below product names and codes: a) X-SCRIBE CPI KIT WIRELESS USB 608 MHz,…
Potential distortion identified in electrocardiogram (ECG) readings when the Source Consistency Filter (SCF) is enabled.
FDA · DeviceBaxter Healthcare CorporationUnited States (including Puerto Rico), Canada, Australia, Bangladesh, Brunei,…Official notice → - US
BioFire Diagnostics, LLC recalls The BIOFIRE Respiratory Panel 2.1 (RP2.1) is a PCR-based multiplexed nucleic acid test intended for use with the BIOFIRE FILMARRAY 2.0…
A manufacturing event may contribute to elevated rates of false negative results while using gastrointestinal panel and respiratory panel, which could lead to inappropriate antibiotic treatment, no treatment, delay of…
FDA · DeviceBioFire Diagnostics, LLCUS: NC, MO, NE, CT, IL, TN, NJ, OH, MA, CA, FL, UT, IA, KS, TX, MDOfficial notice → - US
Immunostics, Inc. recalls Detector H. Pylori, Catalog Number IHP-30
Labeling for affected lots incorrectly indicates the expiration date is 10/31/2023. However, the correct expiration date is 10/31/2022. Use of the product after its expiration may cause false positive, false negative,…