Drugs & medicalClass II

CooperSurgical, Inc. recalls NEO-fit Neonatal Endotracheal Tube Grip, Part Number 42-2540

Firm has received 11 complaints involving a loose or detached metal clips, including 3 cases where the metal clip was ingested by the patient, and 3 cases where the metal clip was removed from the patient's mouth. In…

Read the official notice →
Date
2022-11-16
Country
United States
Brand
CooperSurgical
Product
NEO-fit Neonatal Endotracheal Tube Grip, Part Number 42-2540
Classification
Class II
Units
Worldwide distribution: US (Nationwide) including Puerto Rico; and countries…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 CooperSurgical recalls

  1. 2023-12-13
  2. US
    Drugs & medicalClass II

    CooperSurgical, Inc. recalls Cooper Surgical H/S ELLIPTOSPHERE CATH 5 Fr -For administering contrast media during Hysterosalpingography or Hysterosonography procedures…

    Incorrect bonding material used for assembly of the catheter, may fail, resulting in detachment of component parts, broken components, or leakage. This breakage may result in delay of procedure

    FDA · DeviceCooperSurgical, Inc.Nationwide Foreign: BELGIUM CANADA MALAYSIA NETHERLANDS SPAIN SWEDEN SWITZERLANDOfficial notice →
  3. 2023-04-12
  4. US
    Drugs & medicalClass II

    CooperSurgical, Inc. recalls Global Total LP single step medium, 60mL, bicarbonate-buffered media for D1-5 embryo culture and transfer, Reference Number H5GT-060

    It has come to CooperSurgical's attention that the affected Product may contain a medium other than the Global Total LP single step medium which does not contain the protein source required for embryo culture and…

    FDA · DeviceCooperSurgical, Inc.Worldwide - US Nationwide distribution in the states of NY, UT and the…Official notice →
  5. 2023-02-08
  6. US
    Drugs & medicalClass II

    CooperSurgical, Inc. recalls BIOPSY MEDIUM 10ML, Reference Number 10620010 A, used for blastomere biopsy of cleavage stage embryos for Pre-implantation Genetic…

    The affected product may contain a medium other than the Biopsy Medium. There is a risk that use of the Product from this lot could cause degradation of the embryo.

    FDA · DeviceCooperSurgical, Inc.Global Distribution including countries of: Bahrain, Belgium, Bulgaria, Egypt,…Official notice →
  7. 2022-10-05
  8. US
    Drugs & medicalClass II

    CooperSurgical, Inc. recalls Humidifier bottle and syringe filter kit (6 count of each) for the BT37 Mark II Benchtop Incubator (AY200246)

    There is a potential breach to the sterile barrier containing the Humidifier Bottles due to the packaging of the filter box located inside the bottle packaging. Damage to the sterile barrier may result in use of an…

    FDA · DeviceCooperSurgical, Inc.Domestic distribution to the following states: AL AZ CA CT DE FL GA HI IL KS…Official notice →
  9. 2022-07-27
  10. US
    Drugs & medicalClass II

    CooperSurgical, Inc. recalls LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055

    There was translation error in the Spanish version of the IFU where the Spanish version instructs the user to leave the blastocyte to air thaw for 5 minutes rather than the correct 5 seconds as indicated in the English…

    FDA · DeviceCooperSurgical, Inc.Domestic: USA AL, AZ, CA, CT, FL, GA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MT,…Official notice →
  11. 2022-05-25
  12. US
    Drugs & medicalClass II

    CooperSurgical, Inc. recalls VITRIGUARD, CARRIER, CLEAR; Model. No. 43782001 The VitriGuard device is a cryopreservation storage device composed of a stick and cap.

    Products in this lot may have compromised barrier seals, introducing a risk to sterility.

    FDA · DeviceCooperSurgical, Inc.Domestic distribution to AZ, CA, FL, IL, MI, MO, NY, OR, TX, and WV. No…Official notice →
All 17 CooperSurgical recalls →

Other drugs & medical recalls in the United States

  1. 2022-11-23
  2. US
    Drugs & medicalClass II

    ImprimisRx NJ recalls Timolol-Latanoprost (0.5/0.005%) ophthalmic drops, Compounded, 5 mL bottle, Imprimis Rx, Ledgewood, NJ.

    Subpotent Drug: The batches contain less than 90% of the labeled amount of latanoprost.

    FDA · DrugImprimisRx NJNationwide in the USAOfficial notice →
  3. US
  4. 2022-11-16
  5. US
    Drugs & medicalClass II

    Boston Scientific Corporation recalls ORISE Gel Submucosal Lifting Agent--Indicated for use in gastrointestinal endoscopic procedures for submucosal lift of polyps,…

    ***Update12/13/22***:Product removal due to higher incidence of adverse events of foreign body reactions*** Potential outcomes associated with foreign body reaction to remnant ORlSE Gel post procedure. Foreign body…

    FDA · DeviceBoston Scientific CorporationWorldwide Distribution: US (Nationwide) and (Foreign) countries of: Algeria…Official notice →
  6. US
    Drugs & medicalClass II

    X-NAV Technologies, LLC recalls X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or performing XMark registration. Catalog…

    Product missing one of two welds connecting the tip to the shaft, if the remaining weld breaks, it is possible that the tip could fall out during X-Mark registration and fall into the patient s mouth. In this case, the…

    FDA · DeviceX-NAV Technologies, LLCUS Nationwide distribution and Foreign country of: CanadaOfficial notice →
  7. US
    Drugs & medicalClass II

    Ortho-Clinical Diagnostics, Inc. recalls VITROS Chemistry Products Calibrator Kit 9 -(GEN) 22 of VITROS PHYT Slides For in vitro diagnostic use only. Product Code:…

    Calibration disk Data Release Version (DRV) 6194 to 6200 contain inappropriate calibration mathematics for VITROS Calibration Kit 9 for calibrating VITROS PHYT Slides, for all lots of slide generation 22 (GEN 22). The…

    FDA · DeviceOrtho-Clinical Diagnostics, Inc.Worldwide Distribution: US (Nationwide) and Countries (Foreign) including:…Official notice →
  8. US
    Drugs & medicalClass II

    Access Vascular, Inc. recalls Scalpel and StatLock included with HydroPICC Catheter Kit - PICC-142, Peripherally Inserted Central Catheter

    Scalpel and StatLock components packaged with specific lots of the HydroPICC catheter have a shorter expiration date than what is listed on the outer kit package.

    FDA · DeviceAccess Vascular, Inc.Domestic distribution to NC, RI, NJ, and IL. No foreign distribution.Official notice →
See all drugs & medical recalls →