Z-2619-2025Class II

Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080

Name: Z-2619-2025 Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080
Creator: Biomet, Inc.
Published: 2025-09-09
License: https://open.fda.gov/license/

Zimmer GmbH / initiated 2025-09-09 / Open, Classified / root cause: labeling and UDI

FDA source

Biomet, Inc. began a recall of Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080 on 2025-09-09. FDA classified it as Class II and gives the reason as "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". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-2619-2025
Classification: Class II
Status: Open, Classified
Initiated: 2025-09-09
Posted: 2025-09-23
Recalling firm: Zimmer GmbH
Product: Juggerknot Mini Soft Anchors, Model/Catalog Number: 912080
Product code: MBI Fastener, Fixation, Nondegradable, Soft Tissue
Reason for recall: 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.
Root cause tag: labeling and UDI
FDA root cause: Under Investigation by firm
Action: An URGENT MEDICAL DEVICE RECALL notification letter dated 9/9/25 was sent to customers. Risk Manager Responsibilities: 1. Review this notification and ensure that affected personnel are aware of the contents. 2. If you have affected product at your facility, assist your Zimmer Biomet sales representative and quarantine all affected product. Your Zimmer Biomet sales representative will remove the affected product from your facility. 3. If the product has been further distributed, provide your customers with the recall notice and ensure documentation. 4. Complete Attachment 1 Certificate of Acknowledgement and send to [email protected]. This form shall be returned even if you do not have affected products at your facility. 5. Retain a copy of the acknowledgement form with your recall records in the event of a compliance audit of your facility s documentation. 6. If you have further questions or concerns after reviewing this notice, please call customer service at 574-371-3071 between 8:00 am and 5:00pm EST, Monday through Friday. Calls received outside of call center operating hours will receive a voicemail prompt or be transferred to an on-call representative in the event of an emergency. Alternatively, your questions may be emailed to [email protected]. Distributor Responsibilities: 1. Review this notification and ensure that affected team members are aware of the contents. 2. Immediately locate and quarantine affected product in your inventory. 3. Immediately return all affected product from your distributorship and from affected hospitals within your territory. a. Complete Attachment 1 Inventory Return Certification Form for each return and send to [email protected]. This form must be returned even if you do not have affected products available to return in your territory. b. Include a hardcopy of Attachment 1 in each carton of your return shipment for immediate processing. c. M
Quantity in commerce: 40
Distribution: US Nationwide distribution.
Product codes and lots: UDI-DI: 00880304520950; Lot Number 0002713620

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2619-2025
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2619-2025	Class II	Ongoing	Voluntary: Firm initiated	2025-10-01	2025-09-23

Product code MBI

K110879Class IIBiomet Sports Medicine Juggerknot (Tm) Mini Soft AnchorBiomet Sports Medicine / cleared 2011-08-19

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)