Drugs & medicalClass I

Kinova Inc recalls KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco replaces the…

Potential installation issue that could result in a fire hazard in the event of an interaction between a damaged Jaco arm and a wheelchair exhibiting electrical leakage.

Read the official notice →
Date
2024-10-23
Country
United States
Brand
Kinova Inc
Product
KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco replaces the…
Classification
Class I
Units
Worldwide - US Nationwide distribution in the states of California, Missouri,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. 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.

Other drugs & medical recalls in the United States

  1. 2024-10-23
  2. US
    Drugs & medicalClass II

    Stryker Corporation recalls 1.2mm Cross Cut Fissure - Intended for use in the cutting, drilling, reaming, decorticating, shaping and smoothing of bone, bone cement…

    May exhibit endotoxin levels greater than 2.15 EU/device, fever and inflammation may occur from endotoxin exposure and meningitis may only occur if there is contact with cerebrospinal fluid and thus,…

    FDA · DeviceStryker CorporationWorldwide distribution - US Nationwide and the countries of Canada, Columbia.Official notice →
  3. US
    Drugs & medicalClass II

    Merit Medical Systems, Inc. recalls Melrose Wakefield Hospital REF K05T-2159 Injector And Syringe, Angiographic/Syringe, Balloon Inflation - The 30 ATM Monarch syringe…

    Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier.

    FDA · DeviceMerit Medical Systems, Inc.Worldwide - U.S. Nationwide distribution including in the states of AL, AR,…Official notice →
  4. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls EVIS EXERA III Video System Center Model Number CV-190. Intended to be used with OLYMPUS camera heads, endoscopes, light…

    Certain serial numbers of the CV-190 do not start up properly because parts that deviated from the specification were assembled into the power supply unit.

    FDA · DeviceOlympus Corporation of the AmericasUS Nationwide distribution.Official notice →
  5. US
    Drugs & medicalClass I

    DATEX--OHMEDA, INC. recalls GE Heathcare Giraffe OmniBed; neo natal incubator

    GE HealthCare has become aware that for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices, the screw that secures the doors that cover the warmer heaters may not have been torqued to specification. This…

    FDA · DeviceDATEX--OHMEDA, INC.Worldwide distribution.Official notice →
  6. US
    Drugs & medicalClass II

    Wilson-Cook Medical Inc. recalls Cook Medical Hemo-7 Hemospray Endoscopic Hemostat, REF G56572, 2.8 mm, Sterile; and Hemo-10 Hemospray Endoscopic Hemostat, REF G21049,…

    Specific lots of product have been manufactured with nonconforming raw materials.

    FDA · DeviceWilson-Cook Medical Inc.Distribution was nationwide. There was government and military distribution.…Official notice →
  7. US
    Drugs & medicalClass II

    Zhejiang Jingwei Pharmaceutical Co., Ltd. recalls First Aid Antiseptic Ointment, Povidone Iodine USP 10%, Inactive Ingredients: mineral oil, petrolatum. NET Wt. 1 OZ…

    Incorrect/Undeclared Excipients: The inactive ingredients labeled on the product boxes and tubes are listed as "mineral oil , petrolatum ". The inactive ingredients in the actual product are polyethylene glycol 400 ,…

    FDA · DrugZhejiang Jingwei Pharmaceutical Co., Ltd.Distributed to one wholesaler in OH for Nationwide distribution.Official notice →
See all drugs & medical recalls →