Tecfen Medical recalls Brand Name: Tecfen Medical Product Name: 3.2mm Slit Knife, Angled Model/Catalog Number: QKN3261 Software Version: No software Product…
Sterility assurance for Ophthalmic knives.
Read the official notice →- Date
- 2025-06-18
- Country
- United States
- Brand
- Tecfen Medical
- Product
- Brand Name: Tecfen Medical Product Name: 3.2mm Slit Knife, Angled Model/Catalog Number: QKN3261 Software Version: No software Product…
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of Connecticut 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
Other drugs & medical recalls in the United States
- 2025-06-18
USBaxter Healthcare Corporation recalls 2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope handles, Product Code 72600
The replacement rechargeable batteries inserted into the Welch Allyn PocketScope handles have the potential to cause a short circuit in the handle, which can lead to exposure to excessive heat and user burns.
- US
Microbiologics Inc recalls KWIK-STICK, Quality control kit for culture media, Catalog Numbers 01065K, Oligella urethralis derived from ATCC¿ 17960; 0621K,…
Affected products were packaged with the incorrect KWIK STIK assembly resulting in the product containing the wrong microorganism. 0621K was packaged 01065K swabs; 01065K was packaged with 0621K swabs. This may lead to…
FDA · DeviceMicrobiologics IncUS Nationwide distribution in the states of California and Pennsylvania and…Official notice → - US
Contamac Solutions, Inc. recalls Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Contact lens insertion solution may lack sterility.
FDA · DeviceContamac Solutions, Inc.US Nationwide distribution in the states of AZ, CA, CO, FL, IL, IN, KS, KY,…Official notice → - US
Ortho-Clinical Diagnostics, Inc. recalls Brand Name: Solana¿ Bordetella Complete Assay Product Name: Solana Bordetella kit Model/Catalog Number: M308 Software Version:…
It was determined that there could be a false positive rate of up to 16.7% for the affected lots associated with the Bordetella parapertussis (BPP) results (only) of the assay.
FDA · DeviceOrtho-Clinical Diagnostics, Inc.Please see the attached list "Consignee List_CL2025-120." Note: This file…Official notice → - US
Remel, Inc recalls Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse Blood, REF CP11410; invitro diagnostic…
Product may have an off color affecting perfomance
FDA · DeviceRemel, IncWorldwide - US Nationwide distribution in the states of AL, GA, KY, VA and the…Official notice → - US
Stryker GmbH recalls Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.
Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail.
FDA · DeviceStryker GmbHWorldwide - US Nationwide distribution in the states of California and…Official notice →