CooperSurgical, Inc. recalls Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075
Coagulate function may not operate with the use of the Hand Switch, failure of the device to coagulate tissue may lead to a prolonged procedure requiring medical intervention to control any intraoperative bleeding and…
Read the official notice →- Date
- 2021-11-24
- Country
- United States
- Brand
- CooperSurgical
- Product
- Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075
- Classification
- Class II
- Units
- US Nationwide Distribution Foreign: ARMENIA, BOLIVIA, CAMBODIA, CANADA, CHILE,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 CooperSurgical recalls
- 2022-11-16
USCooperSurgical, 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…
FDA · DeviceCooperSurgical, Inc.Worldwide distribution: US (Nationwide) including Puerto Rico; and countries…Official notice →- 2022-10-05
- US
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 → - 2022-07-27
- US
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 → - 2022-05-25
- US
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 → - 2022-02-23
- US
- 2021-11-24
- US
CooperSurgical, Inc. recalls Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075-05W
XXX
FDA · DeviceCooperSurgical, Inc.US Nationwide Distribution Foreign: ARMENIA, BOLIVIA, CAMBODIA, CANADA, CHILE,…Official notice →
Other drugs & medical recalls in the United States
- 2021-11-24
- US
Smith & Nephew, Inc. recalls Smith and Nephew EVOS Self-Tapping Locking Screw SST: (1)REF 72413575, 3.5MM x 75MM, and (2) REF 72413570, 3.5MM X 70MM. Sterile.
The labels on the packages of screws were switched.
FDA · DeviceSmith & Nephew, Inc.Distribution was made to AL, AZ, CA, CO, CT, FL, GA, IL, IN, KY, LA, MA, ME,…Official notice → - US
TiSport, Llc recalls Permobil TiLite, Models: Aero Z, and ZRA
Some affected wheelchairs, with transit tie downs, that are used as a passenger seat in a motor vehicle may not be configured in the right orientation to perform as intended if involved in a motor vehicle accident.…
FDA · DeviceTiSport, LlcUS Nationwide Distribution: MD, PA, VA, IN, NY, MO, AR, NE, NJ, WA, NM, IL,…Official notice → - US
CooperSurgical, Inc. recalls Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075-05W
XXX
FDA · DeviceCooperSurgical, Inc.US Nationwide Distribution Foreign: ARMENIA, BOLIVIA, CAMBODIA, CANADA, CHILE,…Official notice → - US
ROi CPS LLC recalls REGARD Vitrectomy Tray
Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of Specifications was used as a component in some of the ROI CPS, LLC products.
- US
Fujifilm Irvine Scientific, Inc. recalls Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage of human oocytes (MII),…
Due to a component in kit being labeled with the incorrect Expiration Date
FDA · DeviceFujifilm Irvine Scientific, Inc.Worldwide Distribution: U.S. (nationwide) to states of: AL, AK, AZ, CA, CT,…Official notice → - US
Ortho-Clinical Diagnostics, Inc. recalls VITROS Immunodiagnostic Products Anti-HBc IgM Controls, Product Code 6801427 For use in monitoring the performance of the VITROS…
Ortho Clinical Diagnostics confirmed a complaint that some VITROS Immunodiagnostic Products Anti-HBc IgM Controls Lot 1690 Controls Values booklet contained information for the incorrect product. While the accuracy of…
FDA · DeviceOrtho-Clinical Diagnostics, Inc.US (Domestic) distribution to states of: AZ, CA, CO, CT, FL, GA, LA, MA, MO,…Official notice →