Vortex Surgical Inc. recalls Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25
Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps…
Read the official notice →- Date
- 2024-02-07
- Country
- United States
- Brand
- Vortex Surgical
- Product
- Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of OH, WA, MN, MI, IA and…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Vortex Surgical recalls
- 2026-02-11
USVortex Surgical Inc. recalls Vortex Surgical TID Pharos Illuminated Depressor, VS0801B
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FDA · DeviceVortex Surgical Inc.Worldwide Distribution: US (nationwide) to states of: AL, AR, AZ, CA, CT, FL,…Official notice →- US
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There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.
FDA · DeviceVortex Surgical Inc.Worldwide Distribution: US (nationwide) to states of: AL, AR, AZ, CA, CT, FL,…Official notice → - 2026-01-07
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Vortex Surgical Inc. recalls Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
Other drugs & medical recalls in the United States
- 2024-02-14
- US
- 2024-02-07
- US
THOR Photomedicine Ltd recalls NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL
One of the ball studs attaching a gas strut to the canopy may fail. There is potential risk of injury should a ball stud fail when someone is in the NovoTHOR and trying to open or close the canopy
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Draegerwerk Ag & Co. Kgaa recalls Atlan, Gas Machine for Anesthesia or Analgesia, Catalog numbers 8621500 (Atlan A350) and 8621600 (Atlan A350 XL)
Internal backup battery may fail spontaneously while the Atlan is being operated without AC mains supply, resulting in unexpected shutdown of the device while running on batteries.
FDA · DeviceDraegerwerk Ag & Co. KgaaNo devices were distributed to end-users (customers) in the US. All devices…Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not…
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Philips North America recalls Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin…
- US
Olympus Corporation of the Americas recalls EZDilate Wire Guided Balloon 6-7-8. indicated for endoscopic dilation of strictures in the alimentary tract in adults and…
Product balloon issues: inflating, deflating and/or retrieving the devices; reports of bursting and leaking and events involving foreign body in patient and prolonged procedure.
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