Getinge Usa Sales Inc recalls ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4
The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational…
Read the official notice →- Date
- 2024-07-17
- Country
- United States
- Brand
- Getinge Usa Sales
- Product
- ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4
- Classification
- Class II
- Units
- Domestic: KY, NC, NY, VA. International: Australia, Bulgaria, Croatia, Czech…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Getinge Usa Sales recalls
- 2025-02-19
USGetinge Usa Sales Inc recalls Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, Flow-c, Flow-e. For…
Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of…
FDA · DeviceGetinge Usa Sales IncDomestic distribution to Kentucky and Connecticut.Official notice →- 2024-11-20
- US
Getinge Usa Sales Inc recalls MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical…
Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may…
FDA · DeviceGetinge Usa Sales IncWorldwide distribution - US Nationwide and the countries of Australia,…Official notice → - 2024-06-12
- US
Getinge Usa Sales Inc recalls Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i C40, Flow-c, Flow-e.
Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of…
FDA · DeviceGetinge Usa Sales IncDomestic: CA, CO, IN, MO, OR, VA, WA. International: Aruba, Australia,…Official notice → - 2024-02-14
- US
Getinge Usa Sales Inc recalls Flow-c Anesthesia System, model 6887700
Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous…
FDA · DeviceGetinge Usa Sales IncWorldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO,…Official notice → - 2024-01-24
- US
Getinge Usa Sales Inc recalls Maquet PowerLED/HLED and PowerLED300 OR Light Systems, Model Numbers and Catalog Numbers EPS MB1 - ARDINT059002A, EPS MB1 - ARDINT059002C,…
A potential for a light system to fall in the operating room.
- 2023-10-11
- US
Getinge Usa Sales Inc recalls Meera Mobile Operating Table-to support and position the patient immediately before, during and after surgical interventions as well as…
Under certain conditions, an issue might prevent the device from performing as intended. A specific sequence of commands on the control unit activates the traction drive and triggers an unintended driving (autodrive)…
Other drugs & medical recalls in the United States
- 2024-07-17
- US
GE Vingmed Ultrasound As recalls GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW
GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and demographics can be displayed on the ultrasound scanner…
- US
Baxter Healthcare Corporation recalls Trulight 5000/3000 Surgical Light, model numbers: a) 4038210 (Duo Surgical Lights}; b) 4038310 (Trio/Quad Surgical Lights)
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and…
- US
American Contract Systems Inc recalls TOTAL KNEE - 302497- Procedure tray Catalog Number: ANTK12AF
Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding component exceeded the residual limits for permanent exposure devices as indicated by ANSI/AAMI/ISO 10993-7/(R)2012.
- US
Ontact Inc recalls 24K Premium Lense, Distributed by Updream Inc.
Contact lenses recalled due to potential bacterial contamination.
FDA · DeviceOntact IncUS Nationwide distribution in the states of California and Nevada.Official notice → - US
Silkprousa LLC recalls Pink Luminous Breast, Breast transilluminator
Firm is marketing and distributing the Pink Luminous Breast device without premarket approval
- US
Synergetics Inc recalls BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)
Sterilization certificates could not be validated by the supplier