Recall Z-2156-2020

Biomet, Inc. · initiated April 17, 2020

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Knee Products: TMJPM-1510 Microfixation Custom Made Device, Left PM-TMJ Model (01)00841036226534(17)220111(10)735550 Product Usage: Knee prosthesis

Codes / lots: Lot Number/UDI: 735550 (01)00841036226534(17)220111(10)735550

Reason for recall

Potential presence of elevated endotoxin levels that exceed the specification limit

FDA-determined cause: Process control

Action taken

Zimmer Biomet issued Urgent Medical Device recall letter dated April 17, 2002 to distributors with direct sales and/or field inventory via email and traceable letter sent via FedEx. Hospitals with direct sales or current inventory, as well as hospitals that have consumed products will be notified via FedEx. Surgeons that have consumed products will be notified via FedEx. Action to take: 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 and send to CorporateQuality.PostMarket@zimmerbiomet.com within three (3) days. This form must be returned even if you do not have affected products available to return in your territory. b. For international returns, request an IRA by emailing zimmerbiometintlirarequests@zimmerbiomet.com c. For each return, send a copy of Attachment 1 to CorporateQuality.PostMarket@zimmerbiomet.com. CF04107 Rev. 4, Eff. Date: 16 Jul 2019 Ref. CP04102 Field Action Activities d. Include a hardcopy of Attachment 1 in each carton of your return shipment for immediate processing. e. Mark RECALL on the outside of the returned cartons. 4. Return the Additional Accounts form to CorporateQuality.PostMarket@zimmerbiomet.com. a. Review the list of hospitals and/or surgeons included with the email notification sent to your facility, which includes a list of hospitals and/or surgeons that have already been notified of this recall. b. Identify whether there are any additional hospitals and/or surgeons that Zimmer Biomet has not notified and list these accounts on the Additional Accounts form. Please provide the form in Excel format. c. If there are no additional accounts or surgeons to notify, please indicate that there are no additional accounts, or i

Details

Recall number
Z-2156-2020
Initiated
April 17, 2020
Terminated
June 25, 2021
Quantity
1
Distribution
Worldwide distribution - US Nationwide distribution and the countries of Canada, AHMADABAD, GUJARAT, BANGKOK, BELROSE NSW, BUENOS AIRES, CHILE, COSTA RICA, HIRATSUKA CITY, HUECHURABA SANTIAGO, INDIA, JAPAN, MEXICO DF, NETHERLANDS, PICHINCHA, EC, SAN JOSE, SINGAPORE, TAIWAN, THAILAND, YONGSAN-GU SEOUL.
Recalling firm
Biomet, Inc., Warsaw, IN

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-2144-2020 Class IIExtremities Item Number: 1)113954 Hybrid Glenoid Glenoid Base, 4 MM 2) XL-115366…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated
Z-2145-2020 Class IIHip Products Item Number: 1) 110010462 RingLoc Hip System, Acetabular Bi-Polar Cup, 28…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated
Z-2146-2020 Class IIKnee Products: 141356 Regenerex Series-A Patella 3 Peg, 31 MM 141358 Regenerex Series-A…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated
Z-2147-2020 Class IIKnee Products: 150414 Orthopedic Salvage System (OSS) Tibial Bearing, 20 MM Standard -…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated
Z-2148-2020 Class IIKnee Products: 154335 Oxford Partial Knee System, Fixed Lateral Tibial Construct, Left…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated
Z-2149-2020 Class IIKnee Products: 155308 Knees AGC Knee System PS Molded Tibial Component, 10 MM X 65 MM…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated
Z-2150-2020 Class IIKnee Products: 183622 Vanguard Knee System PS Tibial Bearing, 12 MM X 63/67 MM 183620…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated
Z-2151-2020 Class IIKnee Products: 189260 Vanguard Knee System, CR-L Mono Lock Tibial Bearing, 10 MM X 71 MM…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated
Z-2152-2020 Class IIKnee Products: 189420 Vanguard Knee System, PS Mono Lock Tibial Bearing, 10 MM X 63 MM…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated
Z-2153-2020 Class IIKnee Products: 183742 Vanguard Knee System, PS+ Tibial Bearing, 12 MM, 71/75 MM…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated
Z-2154-2020 Class IIKnee Products: 184762 Knees Vanguard Knee System, Series-A Standard Patella, 28 MM…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated
Z-2155-2020 Class IIKnee Products: US154709 Knees Vanguard M Partial Knee System MonoBlock Tibial Tray…Potential presence of elevated endotoxin levels that exceed the specification limit 04/17/2020Terminated