Zimmer Surgical Inc
Complete recall history across all FDA and CPSC categories — 26 total recalls
Zimmer Surgical Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (26)
FDA medical device enforcement actions by Zimmer Surgical Inc
| Date | Product | Reason | Class |
|---|---|---|---|
| Dec 24, 2025 | Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tournique... | Device user interface (screen) may freeze or become unresponsive to touch whe... | Class II |
| Dec 24, 2025 | Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tournique... | Device user interface (screen) may freeze or become unresponsive to touch whe... | Class II |
| Nov 24, 2025 | Zimmer Dermatome AN, Model/Catalog Number: 88710100 | The devices may have a misaligned thickness control bar. | Class II |
| Nov 24, 2025 | Zimmer Air Dermatome, Model/Catalog Number: 00880100100 | The devices may have a misaligned thickness control bar. | Class II |
| Jan 2, 2024 | 3:1 Dermacarrier, Model Number 00219501300, skin graft carrier | Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridg... | Class II |
| Sep 5, 2023 | Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the d... | Skin grafts thin and non-uniform when using the affected blades. The issue wo... | Class II |
| Jan 3, 2020 | Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, D... | When inflating/deflating a single bladder, both bladders could potentially in... | Class II |
| Apr 16, 2019 | Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece, & Alva... | Foreign Material in the Alvarado Knee Holder Base Plate Assembly and Foot Pie... | Class II |
| Jun 8, 2018 | Zimmer Dermatone AN, Model No. 88710100 | Devices may have a loose control bar, which could compromise the ability to c... | Class II |
| Jul 27, 2017 | A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be u... | Updated on-device label and 3 pages of an updated Operator/Service Manual. A... | Class II |
| Jul 27, 2017 | A.T.S. 2200TS Tourniquet Systems, Personalized Pressure. Zimmer Surgical, In... | Updated on-device label and 3 pages of an updated Operator/Service Manual. A... | Class II |
| Jul 4, 2016 | Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device... | Zimmer Biomet Surgical has received product complaints reporting that the sur... | Class II |
| Jul 4, 2016 | Zimmer¿ Air Dermatome II Width Plate, 1 in., item number 00-8851-201-00 . ... | The surface coating applied to the device is blistering, peeling and discolor... | Class II |
| Jul 4, 2016 | Zimmer¿ Air Dermatome II Width Plate, 4 inch. Part #00-8851-204-00. Width pla... | The surface coating applied to the device is blistering, peeling and discolor... | Class II |
| Jul 4, 2016 | Zimmer¿ Air Dermatome II Handpiece, item number 00-8851-001-00. The Zimme... | The surface coating applied to the device is blistering, peeling and discolor... | Class II |
| Jul 4, 2016 | Zimmer¿ Air Dermatome II Width Plate, 3 inch. Part #00-8851-203-00. Width pla... | The surface coating applied to the device is blistering, peeling and discolor... | Class II |
| Jul 4, 2016 | Zimmer¿ Air Dermatome II Width Plate, 1.5 inch. Part #00-8851-215-00. Wid... | The surface coating applied to the device is blistering, peeling and discolor... | Class II |
| Jul 4, 2016 | Zimmer¿ Air Dermatome II Handpiece w/o Hose, item number 00-8851-001-01. T... | The surface coating applied to the device is blistering, peeling and discolor... | Class II |
| Jul 4, 2016 | Zimmer¿ Air Dermatome II Width Plate, 2 inch. Part # 885120200. Width plate i... | The surface coating applied to the device is blistering, peeling and discolor... | Class II |
| Jun 24, 2015 | 18inch Dual Port/Single Bladder Disposable Tourniquet Cuff, Zimmer Surgical, ... | The inside of the folded Instructions For Use (IFU) pamphlet was missing the ... | Class II |
| Jun 24, 2015 | 30inch Dual Port/Single Bladder Disposable Tourniquet Cuff with PLC, Zimmer S... | The inside of the folded Instructions For Use (IFU) pamphlet was missing the ... | Class II |
| Apr 21, 2015 | Zimmer 100 mL Hemovac Device Hemovac Mini Evacuator. 00-2568-000-10. Zimmer... | Devices were placed in a shipper carton without the appropriate number of the... | Class III |
| Oct 6, 2014 | UNIVERSAL Modular Electric/Battery Handpiece for surgery The electric hand... | Non-injury complaints from Europe identified a malfunction that made it possi... | Class II |
| May 7, 2013 | Zimmer Air Dermatome II, REF 00-8851-001-01 handpiece, w/o hose, Rx, non-ste... | This removal is in response to complaints alleging that the Zimmer Air Dermat... | Class II |
| May 7, 2013 | The Zimmer Air Dermatome, REF 00- 8801- 001- 00 , Rx, non-sterile grafti... | This removal is in response to complaints alleging that the Zimmer Air Dermat... | Class II |
| May 7, 2013 | Zimmer Air Dermatome II, REF 00-8851-001-00 handpiece Rx, non-sterile gr... | This removal is in response to complaints alleging that the Zimmer Air Dermat... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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