--- title: "Centinel Spine, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Centinel Spine, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/centinel-spine-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Centinel Spine, Inc. recall records **5** reported ongoing 5 records in this archive. Latest source date Mar 20, 2026. 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 Mar 20, 2026 FDA device enforcement ### [Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement.](https://isitonrecall.com/recall/fda-device-z-2050-2026-prodisc-c-sk-u-s-implant-extra-large-5mm-model-pdsxl5-total-cervical-disc-replacement/) Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, GA, LA, MO, NY, TN, TX. [Official source for Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2050-2026%22) Mar 20, 2026 FDA device enforcement ### [Prodisc C SK U.S. IMPLANT EXTRA LARGE 6MM. Model Number: PDSXL6. Total cervical disc replacement.](https://isitonrecall.com/recall/fda-device-z-2051-2026-prodisc-c-sk-u-s-implant-extra-large-6mm-model-number-pdsxl6-total-cervical-disc-replacement/) Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, GA, LA, MO, NY, TN, TX. [Official source for Prodisc C SK U.S. IMPLANT EXTRA LARGE 6MM. Model Number: PDSXL6. Total cervical disc replacement.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2051-2026%22) Dec 31, 2025 FDA device enforcement ### [Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product Description: Total cervical disc replacement Component: No](https://isitonrecall.com/recall/fda-device-z-1426-2026-brand-name-prodisc-product-name-prodisc-c-sk-model-catalog-number-pdsl6-software-version-n-a-product/) Products were mislabeled as the 6mm product but included the 5 mm product. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, CA, CO, LA, NY, OR, TN, TX. [Official source for Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1426-2026%22) Jul 18, 2024 FDA device enforcement ### [prodisc C SK, Total cervical disc replacement, medical device, Model/Catalog Number: PDSM5](https://isitonrecall.com/recall/fda-device-z-3212-2024-prodisc-c-sk-total-cervical-disc-replacement-medical-device-model-catalog-number-pdsm5/) During the assembly of Prodisc C, a blue discoloration was observed on a Prodisc C inlay. The discoloration is considered a foreign contaminate that may not have been fully evaluated in the manufacturing validations. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for prodisc C SK, Total cervical disc replacement, medical device, Model/Catalog Number: PDSM5](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3212-2024%22) Jul 18, 2024 FDA device enforcement ### [prodisc C SK, Total cervical disc replacement, Model/Catalog Number: PDSM5](https://isitonrecall.com/recall/fda-device-z-3213-2024-prodisc-c-sk-total-cervical-disc-replacement-model-catalog-number-pdsm5/) During the assembly of Prodisc C, a blue discoloration was observed on a Prodisc C inlay. The discoloration is considered a foreign contaminate that may not have been fully evaluated in the manufacturing validations. Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for prodisc C SK, Total cervical disc replacement, Model/Catalog Number: PDSM5](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3213-2024%22) ## Reasons in these listed records - Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm. - Products were mislabeled as the 6mm product but included the 5 mm product. - During the assembly of Prodisc C, a blue discoloration was observed on a Prodisc C inlay. The discoloration is considered a foreign contaminate that may not have been fully evaluated in the manufacturing validations. These examples come from this result page and are not a ranking of every recall reason. ## Checking Centinel Spine, Inc. ### Is there a recall on centinel spine, inc. right now? This archive contains 5 records, including 5 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 Centinel Spine, Inc.](https://isitonrecall.com/check/?q=Centinel%20Spine%2C%20Inc.) 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