Think Surgical, Inc. recalls Think Surgical Square Driver REF: 109126
Robotic system square drive failed to meet design specifications potentially resulting in pin becoming stuck in square driver or the pin wobbling during drilling.
Read the official notice →- Date
- 2026-10-28
- Country
- United States
- Brand
- Think Surgical
- Product
- Think Surgical Square Driver REF: 109126
- Classification
- Class II
- Units
- US Nationwide distribution in the states of NY and DE.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Think Surgical recalls
- 2026-07-15
Think Surgical, Inc. recalls TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI…
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
FDA · DeviceThink Surgical, Inc.U.S. Nationwide distribution in the states of AZ, CA, DE, FL, IA, KS, LA, MI,…Official notice →- 2024-03-27
Think Surgical, Inc. recalls Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System
There is a galling effect (cold-weld) caused by friction between the array fixation pins and the TMINI array guide holes due to insufficient clearance between the outer diameter of the fixation pins and the inner…
FDA · DeviceThink Surgical, Inc.US Nationwide distribution in the states of AL, OH, NV, TX, UT, CA, MO.Official notice →
Other drugs & medical recalls in the United States
- 2026-10-28
Axonics, Inc. recalls PNE Lead Implant Kit REF: 1701
Retroactively Reported: 10mL luer lock syringes included in kit may leak , break or experience other issues that may pose a risk to users.
FDA · DeviceAxonics, Inc.US Nationwide distribution including in the states of FL, AL, NE, CA, NY,MI,…Official notice →Medtronic Navigation, Inc. recalls Medtronic Biopsy Needle Kit, REF: 9733068, Passive, Sterile EO, Rxonly
Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect and track the spheres.
FDA · DeviceMedtronic Navigation, Inc.US: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY KY LA MA MD ME MI MN…Official notice →B Braun Medical Inc recalls B Braun SAFSITE Injection Site, RV1000NC SAFSITE VALVE W/O EXTRA CAP. Catalog Number: 415068.
Potential for leakage and backflow at the Safsite valve.
FDA · DeviceB Braun Medical IncWorldwide - US Nationwide distribution in the states of CA, FL, IL, IN, MN,…Official notice →Abbott recalls Amplatzer Amulet Left Atrial Appendage Occluder Model Numbers 1. 9-ACP2-007-016 2. 9-ACP2-007-018 3. 9-ACP2-007-020 4. 9-ACP2-007-022 5.…
Changes to Instructions for Use (IFU) for the device regarding risk of Pulmonary Artery Injury (PAI).
Philips Ultrasound, LLC recalls Philips Lumify Diagnostic Ultrasound System
Ultrasound system may: 1) Not recognize previous transducer registration, prevent scanning, require re-registration with Wi-Fi/cellular access, which may be unavailable outside of the hospital…
FDA · DevicePhilips Ultrasound, LLCWorldwide - US Nationwide distribution including in the states of CA, MA, IL,…Official notice →Ventec Life Systems, Inc. recalls VOCSN (Japan) Model Number: PRT-01100-100, Package PN:PRT-01126-100. used for ventilatory support.
Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
FDA · DeviceVentec Life Systems, Inc.Distribution US nationwide including Puerto Rico.Official notice →