Full Vision Inc recalls TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA
Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
Read the official notice →- Date
- 2023-07-12
- Country
- United States
- Brand
- Full Vision
- Product
- TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA
- Classification
- Class II
- Units
- USA (Nationwide), Australia, Bahrain, Canada, Chile, Colombia, Costa Rica,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Full Vision recalls
- 2022-12-14
USFull Vision Inc recalls FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 220V, Model #317-07929
This has been identified a rare occurrence, under a specific scenario, where the circuit is found in a latch-up condition on the PCB that controls the safety function of the Magnetic Safety Tether, that when the magnet…
Other drugs & medical recalls in the United States
- 2023-07-12
- US
Waldemar Link GmbH & Co. KG (Mfg Site) recalls LinkSymphoKnee Distal Femoral Augment - Tilastan - Size. 7-8, Lateral-Right/Medial-Left, 5mm-Intended for primary and…
Fixation screw was inserted through the wrong side of the augment (distal to proximal, as opposed to proximal to distal, which is the correct orientation).
FDA · DeviceWaldemar Link GmbH & Co. KG (Mfg Site)US Nationwide distribution in the states of AL, IL, IN, LA, GA, NV, TX.Official notice → - US
T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. recalls Betta Link LG Reusable Fishmouth Guide-Intended for use in soft tissue to bone fixation in the repair of the natural…
Drill guides might bend when axial forces are applied by surgeon during procedure and result in potential metal shavings due to friction with the drill bit.Risk to patients includes potential of injury.
FDA · DeviceT.A.G. MEDICAL PRODUCTS CORPORATION, LTD.Worldwide distribution - US Nationwide and the countries of Australia, Japan,…Official notice → - US
Intuitive Surgical, Inc. recalls da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12
Fenestrated Graspers have a manufacturing issue has the potential to cause breakage on both upper and/or lower grips, which could lead to stainless steel fragments falling into the patient that may be either detected…
FDA · DeviceIntuitive Surgical, Inc.Worldwide - US Nationwide distribution in the states of PR, FL, MN, PA, AZ,…Official notice → - US
GE Healthcare Finland Oy recalls TruSignal Sensitive Skin Sensor, REF TS-SE-3; Oximeter
There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.
- US
QUIDEL CARDIOVASCULAR INC recalls Quidel Triage Cardiac Panel: REF: 97000HS, 97021HS (Troponin I), 97022HS (CK-MB and Troponin I), 97000HSEU, 97000HSEUJP, 97000HZ01,…
Raw material issue may cause cardiac panel products to have an average of 30% troponin signal reduction across measurement range 0.05 ng/mL to 30 ng/mL, QC testing won't detect anomaly, so an alternate method is…
FDA · DeviceQUIDEL CARDIOVASCULAR INCUS: TX, NC, CA, LA, SC, OR, HI, OK, AZ, AL, KS, WA, FL, VA, IA, WV, MT, UT, CO…Official notice → - US
Strides Pharma Inc. recalls Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, Rx Only, Manufactured by: Vivimed Life Sciences Private…
Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.