Drugs & medicalClass II

Instrumentation Laboratory recalls GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Na+, K+, Ca++, Part Numbers 00024307507, 00024315007, 00024330007, 00024345007, 00024360007

Internal testing identified that the GEM Premier PAKs (cartridges) may exhibit an over-recovery (i.e., positive bias) of pO2 results in the low range (at pO2 levels less than 60 mmHg) that are outside of labeled…

Read the official notice →
Date
2023-11-29
Country
United States
Brand
Instrumentation Laboratory
Product
GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Na+, K+, Ca++, Part Numbers 00024307507, 00024315007, 00024330007, 00024345007, 00024360007
Classification
Class II
Units
US States: MA, MN, NY. India.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Instrumentation Laboratory recalls

  1. 2025-12-24
  2. US
    Drugs & medicalClass III

    Instrumentation Laboratory recalls HemosIL SynthAFax. Partial Thromboplastin Time Tests.

    Recalled lots were manufactured with double the amount of preservative concentration.

    FDA · DeviceInstrumentation LaboratoryDomestic: CA, CO, FL, NY; Foreign: AR, AT, CA, CZ, DE, DK, ES, FR, GB, IE, IL,…Official notice →
  3. 2025-08-20
  4. US
    Drugs & medicalClass II

    Instrumentation Laboratory recalls HemosIL LMW Heparin Controls; Part Number: 0020300200;

    Multiple complaints indicating lower than expected quality control (QC) results and in some instances QC recovery below the lower limit of the package insert acceptance range when testing is performed with HemosIL…

    FDA · DeviceInstrumentation LaboratoryWorldwide - US Nationwide and the countries of Algeria, Andorra, Argentina,…Official notice →
  5. 2025-02-05
  6. US
    Drugs & medicalClass II

    Instrumentation Laboratory recalls HemosIL Heparin Calibrators; Part Number: 0020300600; in vitro diagnostic

    Control indicating lower than expected quality control (QC) results and in some instances QC recovery below the lower limit of the package insert acceptance range.

    FDA · DeviceInstrumentation LaboratoryWorldwide - US Nationwide and the countries of Andorra, Algeria, Armenia,…Official notice →
  7. 2023-09-20
  8. US
    Drugs & medicalClass II

    Instrumentation Laboratory recalls ACL TOP Family 50 Series Models as follows: In vitro diagnostic clinical use in the hemostasis laboratory for coagulation and/or…

    Sample misidentification could occur under specific conditions and patient management altered based on an incorrectly assigned result

    FDA · DeviceInstrumentation LaboratoryWorldwide distribution - US Nationwide and the countries of Canada, Finland,…Official notice →
  9. 2023-04-05
  10. US
    Drugs & medicalClass II

    Instrumentation Laboratory recalls ACL ELITE Refurbished-Analyzer designed specifically for clinical use in the hemostasis laboratory, for coagulation and/or…

    Removes the test definition for HemosIL Liquid Anti-Xa (PN 0020302600 and 0020302601) from the ACL Elite/Elite Pro instruments

    FDA · DeviceInstrumentation LaboratoryWorldwide distribution - US Nationwide and the countries of Canada, Albania,…Official notice →
  11. 2022-05-18
  12. US
    Drugs & medicalClass II

    Instrumentation Laboratory recalls HemosIL ReadiPlasTin, Part No. 0020301400

    Variable and out of specification QC results with HemosIL ReadiPlasTin. IL will remove all lots from the market and convert customers to an alternative prothrombin time (PT) reagent, specifically HemosIL RecombiPlasTin…

    FDA · DeviceInstrumentation LaboratoryUS Nationwide distribution including in the states of AZ, CA, IA, IL, IN, KS,…Official notice →
All 14 Instrumentation Laboratory recalls →

Other drugs & medical recalls in the United States

  1. 2023-11-29
  2. US
    Drugs & medicalClass II

    Biomet, Inc. recalls Compress Device Short Anchor Plug, 26 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement.…

    Anchor plugs potentially have metal burrs in the transverse holes of the device, preventing the drill or pins from passing through, may result in extension of surgery

    FDA · DeviceBiomet, Inc.Worldwide distribution - US Nationwide and the countries of ARGENTINA,…Official notice →
  3. US
    Drugs & medicalClass II

    SunMed Holdings, LLC recalls Medline manual resuscitators with integrated manometer, multiple accessory configurations to include: 1. Adult Resuscitator REF #s:…

    A backwards leak present in the integrated manometer of the patient valve allows for CO2 rebreathing.

    FDA · DeviceSunMed Holdings, LLCUS Nationwide distribution including in the states of AR, AZ, CA¿CO, CT, FL,…Official notice →
  4. US
    Drugs & medicalClass II

    Avanos Medical, Inc. recalls AVANOS BALLARD Closed Suction System for Adults, 14 Fr, DSE, MDI, Product code 221038, provide suction on patients on mechanical ventilation

    Certain lots of BALLARD Closed Suction System for Adults, 14 Fr, DSE, MDI were labeled as not being made with Di(2-ethylhexyl) phthalate (DEHP); however, Avanos has determined that the tubing components of the product…

    FDA · DeviceAvanos Medical, Inc.US and South AfricaOfficial notice →
  5. US
    Drugs & medicalClass II

    Sage Products Inc recalls stryker Sage PrimaFit External Urine Management System for the Female Anatomy

    A small percentage of devices in three lots of product may contain a tape with a natural rubber latex adhesive which is not declared on the label

    FDA · DeviceSage Products IncUS and CanadaOfficial notice →
  6. US
    Drugs & medicalClass II

    Medtronic Neuromodulation recalls Model 97745 Controller used with Models 97715 and 97716 Intellis Neurostimulators

    Units distributed in Korea and Turkey that did not have the correct firmware installed to support the user interface in the local language.

    FDA · DeviceMedtronic NeuromodulationInternational distribution to the countries of S. Korea and Turkey.Official notice →
  7. US
    Drugs & medicalClass II

    BioFire Diagnostics, LLC recalls FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen computer and USB…

    Due to an increased risk of degradation of the power entry switch resulting from arcing inside of the power switch that may result in carbon build-up on the switch contacts. The carbon build-up may lead to excess…

    FDA · DeviceBioFire Diagnostics, LLCWorldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →
See all drugs & medical recalls →