Biomet, Inc. recalls Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080
The outer carton box label is for the JuggerKnot 1.0mm Mini products. However, the products within the carton are JuggerKnot 1.4mm Short devices.
Read the official notice →- Date
- 2025-10-01
- Country
- United States
- Brand
- Biomet
- Product
- Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080
- Classification
- Class II
- Units
- US Nationwide distribution.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Biomet recalls
- 2026-08-12
US
Biomet, Inc. recalls Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description: Intramedullary Bone Saw Blade Assembly 13mm
Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
FDA · DeviceBiomet, Inc.Refer to the attached ZFA 2026-00096_Initial Consignee List and ZFA…Official notice →- 2025-10-29
US
Biomet, Inc. recalls BIOMET ZipTight, Acute AC Joint Implant, Single Ziploop , Model/Catalog Number: 904834; Fixation System for AC Joint Repair
There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single Ziploop
FDA · DeviceBiomet, Inc.Refer to the attached ZFA 2025-00166_Initial Consignee List and ZFA…Official notice →- 2024-11-27
US
Biomet, Inc. recalls JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result in extension of surgery to find another product, or may lead to adverse local tissue reaction leading to…
FDA · DeviceBiomet, Inc.Worldwide distribution - US Nationwide and the countries of Australia, Brazil,…Official notice →- 2024-07-03
US
Biomet, Inc. recalls RingLoc Bi-Polar Hip System Acetabular Cup, 41 mm Outer Diameter - Used in hip hemi-arthroplasty Item Number: 11-165206
41 mm acetabular outer heads were potentially assembled with a 42 mm locking ring, may lead to joint instability leading requiring surgical intervention
FDA · DeviceBiomet, Inc.Worldwide - US Nationwide distribution in the states of AZ, CA, NJ, PA, TX, VA…Official notice →- 2024-05-01
US
Biomet, Inc. recalls Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082. The product is placed into a foil pouch with…
Possible damage to the Vanguard Knee System AS Tibial Bearing caused during the manufacturing process.
FDA · DeviceBiomet, Inc.Worldwide distribution - US Nationwide in the state of IN and the countries of…Official notice →- 2023-12-27
US
Biomet, Inc. recalls Biolox Ceramic Option Head Zimmer 12/14 40mm +0, Item Number 00-8777-040-02
One product complaint was received reporting that there was an incorrect adapter in the packaging. An adapter with neck length M/+0 was inside the product packaging, which should have contained an adapter with neck…
FDA · DeviceBiomet, Inc.US States: AL, CA, MD, MI, NC, OH, OK, TN, TX. Netherlands.Official notice →
Other drugs & medical recalls in the United States
- 2025-10-01
US
Mindray DS USA, Inc. dba Mindray North America recalls BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017, 6660E-PA00014, 6660E-PA00012, 6660E-PA00011,…
Potential for activation of an abnormal alarm pause.
FDA · DeviceMindray DS USA, Inc. dba Mindray North AmericaWorldwide - Nationwide distribution and the country of Canada.Official notice →US
Tandem Diabetes Care, Inc. recalls t:slim X2 Insulin Pump with Interoperable Technology (with Tandem t:slim mobile app)
an app defect that occurs when the phone is set to a right-to-left language, which causes app-pump pairing issues and graphical defects, which can potentially lead to incorrect therapy decisions and subsequent…
FDA · DeviceTandem Diabetes Care, Inc.International distribution to the country of Israel.Official notice →US
Stryker Communications recalls Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034
Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.
FDA · DeviceStryker CommunicationsUS Nationwide distribution in the states of TX, IL, NY, UT, OR, AZ, VT, NY,…Official notice →US
Boston Scientific Corporation recalls Extractor Pro RX Retrieval Balloon Catheter; UPN (REF): (1) M00547030 (9-12mm Below), (2) M00547000 (9-12mm Above);
The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.
FDA · DeviceBoston Scientific CorporationUS Nationwide distribution in the states of CA, CO, GA, ID, IL, IN, MA, ME,…Official notice →US
ORTOMA AB recalls Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight REF 30-201 Model Number: 2001 UDI-DI code: 07350137521019 Inserter Adapter OTD…
Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.
FDA · DeviceORTOMA ABWorldwide - U.S. Nationwide distribution in the state of FL and the countries…Official notice →US
Biofire Defense recalls FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative, multiplexed, nucleic acid-based in vitro diagnostic test intended for use…
FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of internal control failures when testing positive blood culture, which may lead to delayed results and additional diagnostic workup.
FDA · DeviceBiofire DefenseUS Nationwide distribution in the states of AL, AZ, UT, CA, TX, DC , VA, FL,…Official notice →