--- title: "Tyber Medical Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Tyber Medical recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/tyber-medical/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Tyber Medical recall records **20** reported ongoing 20 records in this archive. Latest source date Dec 19, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Dec 19, 2025 FDA device enforcement ### [Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/10Shaft/Left/Std/139mm Model/Catalog Number: 02.426.681S Product Description: 2 Colu...](https://isitonrecall.com/recall/fda-device-z-1131-2026-brand-name-volt-wrist-treatment-system-product-name-2-4-2-7-2column-dist-radius-plate-6hd-10shaft-le/) The supplier manufactured anatomical left plates with an incorrect thread orientation. Class II Reported ongoing Distribution: US Nationwide distribution in the state of PA. [Official source for Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/10Sh...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1131-2026%22) Dec 19, 2025 FDA device enforcement ### [Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/14Shaft/Left/Std/186mm Model/Catalog Number: 02.426.691S Product Description: 2 Colu...](https://isitonrecall.com/recall/fda-device-z-1132-2026-brand-name-volt-wrist-treatment-system-product-name-2-4-2-7-2column-dist-radius-plate-6hd-14shaft-le/) The supplier manufactured anatomical left plates with an incorrect thread orientation. Class II Reported ongoing Distribution: US Nationwide distribution in the state of PA. [Official source for Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/14Sh...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1132-2026%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate, 4-hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708041](https://isitonrecall.com/recall/fda-device-z-1209-2025-a-l-p-s-mvx-anatomic-lat-fib-plate-4h-lt-anatomic-lateral-fibula-plate-4-hole-left-intended-for-fixa/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate, 4-hole, Left Intended...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1209-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate, 4-hole, Right Model/Catalog Number: 770708042](https://isitonrecall.com/recall/fda-device-z-1210-2025-a-l-p-s-mvx-anatomic-lat-fib-plate-4h-rt-anatomic-lateral-fibula-plate-4-hole-right-model-catalog-nu/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate, 4-hole, Right Model/Ca...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1210-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 6H LT- Anatomic Lateral Fibula Plate, 6-hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708061](https://isitonrecall.com/recall/fda-device-z-1211-2025-a-l-p-s-mvx-anatomic-lat-fib-plate-6h-lt-anatomic-lateral-fibula-plate-6-hole-left-intended-for-fixa/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 6H LT- Anatomic Lateral Fibula Plate, 6-hole, Left Intended ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1211-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate, 6-hole, Right Model/Catalog Number: 770708062](https://isitonrecall.com/recall/fda-device-z-1212-2025-a-l-p-s-mvx-anatomic-lat-fib-plate-6h-rt-anatomic-lateral-fibula-plate-6-hole-right-model-catalog-nu/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 6H RT: Anatomic Lateral Fibula Plate, 6-hole, Right Model/Ca...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1212-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate, 8-hole, Left Intended to bridge or otherwise stabilize bone fragments to facilitate healing. Model/Cat...](https://isitonrecall.com/recall/fda-device-z-1213-2025-a-l-p-s-mvx-anatomic-lat-fib-plate-8h-lt-anatomic-lateral-fibula-plate-8-hole-left-intended-to-bridg/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate, 8-hole, Left Intended ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1213-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H RT: Anatomic Lateral Fibula Plate, 8-hole, Right Indicated for use in Fixation of fractures of the distal tibia Model/Catalog Number: 770...](https://isitonrecall.com/recall/fda-device-z-1214-2025-a-l-p-s-mvx-anatomic-lat-fib-plate-8h-rt-anatomic-lateral-fibula-plate-8-hole-right-indicated-for-us/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H RT: Anatomic Lateral Fibula Plate, 8-hole, Right Indicate...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1214-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Anatomic Lateral Fibula Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number: ...](https://isitonrecall.com/recall/fda-device-z-1215-2025-a-l-p-s-mvx-product-name-anatomic-lat-fib-plate-10h-lt-anatomic-lateral-fibula-plate-10-hole-left-in/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX- Product Name: ANATOMIC LAT FIB PLATE 10H LT Anatomic Lateral Fibula Plate, 10-Hole,...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1215-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 10H RT- Anatomic Lateral Fibula Plate, 10-Hole, Right. Intended forFixation of fractures of the distal tibia Model/Catalog Number: 770708102...](https://isitonrecall.com/recall/fda-device-z-1216-2025-a-l-p-s-mvx-anatomic-lat-fib-plate-10h-rt-anatomic-lateral-fibula-plate-10-hole-right-intended-forfi/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 10H RT- Anatomic Lateral Fibula Plate, 10-Hole, Right. Inten...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1216-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate, 12-Hole, Left. Inended for Fixation of fractures of the distal tibia Model/Catalog Number: 770708121](https://isitonrecall.com/recall/fda-device-z-1217-2025-a-l-p-s-mvx-p-anatomic-lat-fib-plate-12h-lt-anatomic-lateral-fibula-plate-12-hole-left-inended-for-f/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate, 12-Hole, Left. Inen...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1217-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula Plate, 12-Hole, Right. Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 77070812...](https://isitonrecall.com/recall/fda-device-z-1218-2025-a-l-p-s-mvx-anatomic-lat-fib-plate-12h-rt-anatomic-lateral-fibula-plate-12-hole-right-intended-for-f/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 12H RT- Anatomic Lateral Fibula Plate, 12-Hole, Right. Inten...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1218-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX-MEDIAL TIBIA PLATE 6H LT-Medial Tibia Plate, 6-Hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770715061](https://isitonrecall.com/recall/fda-device-z-1219-2025-a-l-p-s-mvx-medial-tibia-plate-6h-lt-medial-tibia-plate-6-hole-left-intended-for-fixation-of-fractur/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX-MEDIAL TIBIA PLATE 6H LT-Medial Tibia Plate, 6-Hole, Left Intended for Fixation of f...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1219-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX- MEDIAL TIBIA PLATE 6H RT-Medial Tibia Plate, 6-Hole, Right Model/Catalog Number: 770715062 Intended for Fixation of fractures of the distal tibia](https://isitonrecall.com/recall/fda-device-z-1220-2025-a-l-p-s-mvx-medial-tibia-plate-6h-rt-medial-tibia-plate-6-hole-right-model-catalog-number-770715062/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX- MEDIAL TIBIA PLATE 6H RT-Medial Tibia Plate, 6-Hole, Right Model/Catalog Number: 77...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1220-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX- MEDIAL TIBIA PLATE 10H LT- Medial Tibia Plate, 10-Hole, Left. Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770715101](https://isitonrecall.com/recall/fda-device-z-1221-2025-a-l-p-s-mvx-medial-tibia-plate-10h-lt-medial-tibia-plate-10-hole-left-intended-fixation-of-fractures/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX- MEDIAL TIBIA PLATE 10H LT- Medial Tibia Plate, 10-Hole, Left. Intended Fixation of ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1221-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate, 10-Hole, Right Intended Fixation of fractures of the distal tibia. Model/Catalog Number: 770715102](https://isitonrecall.com/recall/fda-device-z-1222-2025-a-l-p-s-mvx-medial-tibia-plate-10h-rt-medial-tibia-plate-10-hole-right-intended-fixation-of-fracture/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX-MEDIAL TIBIA PLATE 10H RT-Medial Tibia Plate, 10-Hole, Right Intended Fixation of fr...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1222-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX-MEDIAL TIBIA PLATE 12H LT-Medial Tibia Plate, 12-Hole, Left Intended forFixation of fractures of the distal tibia Model/Catalog Number: 770715121](https://isitonrecall.com/recall/fda-device-z-1223-2025-a-l-p-s-mvx-medial-tibia-plate-12h-lt-medial-tibia-plate-12-hole-left-intended-forfixation-of-fractu/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX-MEDIAL TIBIA PLATE 12H LT-Medial Tibia Plate, 12-Hole, Left Intended forFixation of ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1223-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX--MEDIAL TIBIA PLATE 12H RT-Medial Tibia Plate, 12-Hole, Right Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770715122](https://isitonrecall.com/recall/fda-device-z-1224-2025-a-l-p-s-mvx-medial-tibia-plate-12h-rt-medial-tibia-plate-12-hole-right-intended-for-fixation-of-frac/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX--MEDIAL TIBIA PLATE 12H RT-Medial Tibia Plate, 12-Hole, Right Intended for Fixation ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1224-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H LT-Medial Tibia Plate, 16-Hole, Left Intended for Fixation of fractures of the distal tibia Model/Catalog Number: 770715161](https://isitonrecall.com/recall/fda-device-z-1225-2025-a-l-p-s-mvx-medial-tibia-plate-16h-lt-medial-tibia-plate-16-hole-left-intended-for-fixation-of-fract/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H LT-Medial Tibia Plate, 16-Hole, Left Intended for Fixation o...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1225-2025%22) Jan 21, 2025 FDA device enforcement ### [A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H RT -Medial Tibia Plate, 16-Hole, Right Intended Fixation of fractures of the distal tibia Model/Catalog Number: 770715162](https://isitonrecall.com/recall/fda-device-z-1226-2025-a-l-p-s-mvx-medial-tibia-plate-16h-rt-medial-tibia-plate-16-hole-right-intended-fixation-of-fracture/) Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices Class II Reported ongoing Distribution: Nationwide [Official source for A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H RT -Medial Tibia Plate, 16-Hole, Right Intended Fixation of ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1226-2025%22) ## Reasons in these listed records - The supplier manufactured anatomical left plates with an incorrect thread orientation. - Complaints of the locking screw passing through the locking hole intra-operatively during use of the A.L.P.S. mvX Medial Tibia plates and Anatomic Lateral Fibula. r surgical delays have been reported with the use of the devices These examples come from this result page and are not a ranking of every recall reason. ## Checking Tyber Medical ### Is there a recall on tyber medical right now? This archive contains 20 records, including 20 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Tyber Medical](https://isitonrecall.com/check/?q=Tyber%20Medical) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)