Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R, Negus Tonsil Forceps…
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Read the official notice →- Date
- 2025-03-19
- Country
- United States
- Brand
- Aesculap
- Product
- Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R, Negus Tonsil Forceps…
- Classification
- Class II
- Units
- Distribution was made nationwide and to PR. There was also government/military…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Aesculap recalls
- 2026-03-11
USAesculap Inc recalls Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product…
There is the potential for the length of the trocar shaft to be too long.
FDA · DeviceAesculap IncUS Nationwide distribution in the states of AZ, AR, CA, CO, FL, GA, HI, IA,…Official notice →- 2025-11-05
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Aesculap Inc recalls Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER Model/Catalog Number: EK083P Software Version: N/A Product…
It was determined there is the potential of silicone fragments detaching from the yellow sealing component.
FDA · DeviceAesculap IncWorldwide - US Nationwide distribution in the states of AR, AZ, CA, CT, MD,…Official notice → - 2025-10-08
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Aesculap AG recalls AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R.
Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long" and the ELAN 4 FIXED DURAGUARD LONG was labeled as "Standard."
FDA · DeviceAesculap AGUS distribution to Missouri. OUS International distribution to Norway,…Official notice → - 2024-06-19
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Aesculap Inc recalls Aeos Robotic Digital Microscope, Product Code: PV010
Possibility of the robotic arm to drop more than 10cm from its original position after pressing the emergency stop button due to failure of the integrated safety mechanism.
FDA · DeviceAesculap IncUS Nationwide distribution in the states of AR, FL, IL, IN, KY, MI, NC, NE,…Official notice → - 2024-03-13
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Aesculap Inc recalls DISP.HASSON TROCAR 10/110MM, Product Code EK230SU. For use in laparoscopic procedures.
The sterile blister packaging may be damaged, and sterility may be compromised.
FDA · DeviceAesculap IncWorldwide - US Nationwide distribution in the states of KS, NJ and NY. The…Official notice → - 2024-02-07
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Aesculap Inc recalls MB215R - MILLS DUROGRIP TC Micro Needle Holder, straight, 8:, (203 mm), "TC MILLS NDLE HOLDRRND HNDLSTR203MM"
Needle Holder MB215R was inadvertently distributed as MB362R. Similarly, MB362R was distributed as MB215R during the affected distribution date range. The issue may lead to a short delay in procedure.
FDA · DeviceAesculap IncUS Nationwide distribution in the states of CA, CO, FL, ID, KY, MD, MO, MT,…Official notice →
Other drugs & medical recalls in the United States
- 2025-03-19
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ZOLL Medical Corporation recalls Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: G5S-80C; Software Version: NA Product Description: The Powerheart…
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
FDA · DeviceZOLL Medical CorporationDomestic: Nationwide Distribution International: AE, AI, AM, AR, AT, AU, BD,…Official notice → - US
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls COR Disposable Kit, 8 mm. Cartilage Transplant System.
Device is missing the pin in the graft loader component.
FDA · DeviceDePuy Mitek, Inc., a Johnson & Johnson Co.Domestic: Nationwide Distribution; Foreign: Austria, Belgium, Brazil,…Official notice → - US
TruAbutment Inc. recalls Brand Name: TruScan Body, REF CN38-SB Product Name: TruScan Body compatible with CONELOG 3.8 Model/Catalog Number: CN38-SB Software…
Retroactive: Due to defect and quality issues dental scanner may not scan properly/accurately
FDA · DeviceTruAbutment Inc.US: CA, CO, FL, GA, IA, IL, MD, MN, MS, OH, OR, SD, UT, VA, WA, WI OUS: Japan,…Official notice → - US
CardioFocus, Inc. recalls CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial fibrillation. It is introduced percutaneously in the setting of an…
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CareFusion 303, Inc. recalls BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
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