Invacare Corporation recalls Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V
The battery wiring harness on affected wheelchairs may become disconnected during shipment from the factory or during wheelchair use traversing large obstacles or after a jolt or impact to the wheelchair. The…
Read the official notice →- Date
- 2022-06-01
- Country
- United States
- Brand
- Invacare
- Product
- Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide distribution in the states of AK, AR,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Invacare recalls
- 2024-03-13
USInvacare Corporation recalls Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4) BAR5490IVC (5)…
Invacare Homecare & G-Series Bed Components identified with a potential weld defect leads to premature weld failures to occur on these components
- 2023-08-30
- US
Invacare Corporation recalls DOLOMITE GLOSS ROLLATOR - intended to support during walking and may also serve as a resting seat. Model Number(s): 1654807 - DOLOMITE…
Premature failure of the seat during use, the plastic eyelets of the folding mechanism of the device's seat can break, and in a worst-case crossbar also breaks and the Rollator can collapse causing injury to user
- 2022-07-20
- US
Invacare Corporation recalls Invacare Platinum 5NXG Oxygen Concentrator, Model Numbers P5NXG1, P5NXGC1 (Canada specific model)
Between March 2, 2021 and December 31, 2021, the product label used in production did not contain the "Rx Only" statement as required.
FDA · DeviceInvacare CorporationDomestic distribution to the following states: ALASKA ARIZONA CALIFORNIA…Official notice → - 2022-01-12
- US
Invacare Corporation recalls Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: IFX-20R,…
Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the incorrect deceleration profile,…
FDA · DeviceInvacare CorporationWorldwide distribution - US Nationwide and the countries of Canada, Australia,…Official notice →
Other drugs & medical recalls in the United States
- 2022-06-01
- US
Smith & Nephew Orthopaedics GmbH recalls INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
Right nails were anodized, marked, and labelled as left nails and vice versa
FDA · DeviceSmith & Nephew Orthopaedics GmbHDistributed nationwide to GA, OH, IN, TX, CO, MO, TN, CA, NC, PA and…Official notice → - US
Stradis Healthcare recalls Surgical Suture Kit
There is uncertainty about the integrity of the methods used to ensure the sterile barrier integrity.
- US
Medtronic Perfusion Systems recalls Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System; The device is placed in a plastic tray with a snap on plastic lid, the…
Firm detected an increase in complaints related to fractured jaw tips of the Cardioblate Gemini-s.
FDA · DeviceMedtronic Perfusion SystemsWorldwide distribution - US Nationwide distribution in the states of CA, ND,…Official notice → - US
Medtronic Neuromodulation recalls Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200
The Implantable Neurostimulator (INS) cannot communicate with the clinical programmer and/or the patient programmer system.
FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide distribution in the states of AK, AL,…Official notice → - US
TELEFLEX MEDICAL INC recalls (1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732, non-sterile; (3) Gibeck…
Reports received of torn corrugated breathing tubes.
FDA · DeviceTELEFLEX MEDICAL INCWorldwide distribution - US Nationwide distribution in the states of AL, AR,…Official notice → - US
Microbiologics Inc recalls KWIK-STIK" plus: Clostridium perfringens
Labeling error.
FDA · DeviceMicrobiologics IncDistributed US Nationwide to IA, TN and internationally to Mexico, Colombia,…Official notice →