Drugs & medicalClass II

Parker Laboratories, Inc. recalls Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains 12 inner boxes with 50g tubes packaged in each.

Five complaints were received related to viscosity of Tensive Conductive Adhesive Gel Ref 22-60.

Read the official notice →
Date
2024-03-06
Country
United States
Brand
Parker Laboratories
Product
Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains 12 inner boxes with 50g tubes packaged in each.
Classification
Class II
Units
US (Domestic): AZ, CA, FL, NC, NJ, NV, NY, PA, WA, WI. OUS (Foreign): Canada,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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.

More Parker Laboratories recalls

  1. 2024-05-01
  2. US
    Drugs & medicalClass II

    Parker Laboratories, Inc. recalls Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.

    Product demonstrates low viscosity.

    FDA · DeviceParker Laboratories, Inc.Worldwide distribution - US Nationwide in the states of CA, CO, FL, GA, IL,…Official notice →
  3. 2023-08-30
  4. US
    Drugs & medicalClass II

    Parker Laboratories, Inc. recalls Helix Pain Relieving Cream (Menthol 7.4%), packaged in a) 5 gm pouch (NDC 30775-051-01), b) 3 fl. oz. roll-on (NDC 30775-051-03), c) 4…

    CGMP Deviations

    FDA · DrugParker Laboratories, Inc.Nationwide within the United States, Singapore, Korea and Hong KongOfficial notice →
All 3 Parker Laboratories recalls →

Other drugs & medical recalls in the United States

  1. 2024-03-06
  2. US
    Drugs & medicalClass II

    Acumed LLC recalls Acu-Loc and Acu-Loc 2 bone plates, screws and accessories for the following REF: 70-0045 Acu-Loc VDU Plate Standard, Left; 70-0045-S…

    Distribution without Pre-Market Clearance

    FDA · DeviceAcumed LLCWorldwide distribution - US Nationwide and the countries of AE, AR, AU, BE,…Official notice →
  3. US
    Drugs & medicalClass II

    United Orthopedic Corporation recalls USTAR II Knee System : Cemented Curved Stem, RHS Ti Plasma Spray, Reference Numbers: REF: PE25153109 - PE25151109 - 9x125mm,…

    Their is a potential that the implant curved stem may be oriented incorrectly.

    FDA · DeviceUnited Orthopedic CorporationUS: CA,KY, MI, IN, TN, CO, FL, TX, NV, OUS: Switzerland, United Kingdom,…Official notice →
  4. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls Colonoscope, Model Number PCF-H190DL.

    Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration, fluctuation in temperature or severe shock loads.

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

    Integra LifeSciences Corp. recalls Ref No: INS5HND / Integra Cranial access kit (without Prep solutions) Bit and Guard. For access to the subarachnoid space or the…

    A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Therefore, product sterility maybe compromised.

    FDA · DeviceIntegra LifeSciences Corp.Worldwide distribution - US Nationwide and the countries of Austria, Bahamas,…Official notice →
  6. US
    Drugs & medicalClass II

    GRAPHENANO DENTAL SL recalls GRAPHENANO DENTAL G-CAM, Product Codes: a) 95 Multichroma 14LB2, REF GC00089; b) 95 Multichroma 24LA2, REF GC00112; c) 95 Multichroma…

    Machining error on cams renders the device unusable.

    FDA · DeviceGRAPHENANO DENTAL SLUS Nationwide distribution in the state of Utah.Official notice →
  7. US
    Drugs & medicalClass II

    NxStage MDS Corporation recalls NxStage Cartridge Express with Speedswap, Catalog No. CAR-535. An accessory device for facilitating the removal and replacement of a…

    Product is recalled due to reports of blood leaking or spraying from the arterial line on the cartridge.If this failure occurs, a patient may experience uncontrolled blood loss or a healthcare professional could be…

    FDA · DeviceNxStage MDS CorporationUS domestic distribution to Dialysis Centers located in AZ, CA, CO, GA, IL,…Official notice →
See all drugs & medical recalls →