Zimmer Surgical Inc

FDA recalling firm · 15 enforcement events · 28 product records · 2013–2026 · OH

Zimmer Surgical Inc has 15 FDA enforcement events on this register (28 product records) between 2013 and 2026: 15 device; the busiest year was 2015 with 2.

0% of its events are Class I; the most common class is Class II (14). 5 events are listed as ongoing; the recalling firm's address is in OH.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
9 Jun 2026	Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Dual Hose with CPC Connectors Model/Catalog Number: 60-1812-101-00 Software Version: N/A Product Description: Dual Sterile Extension Hose with PLC Connector Component: N/A	Device	Class II	2	Ongoing
24 Dec 2025	Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 60500010100 Software Version: Software version v2.04 or prior are within scope of the recall for A.T.S.¿ 5000TS Product Description: A.T.S 5000TS Tourniquet Systems Component: N/A	Device	Class II	2	Ongoing
24 Nov 2025	Zimmer Air Dermatome, Model/Catalog Number: 00880100100	Device	Class II	2	Ongoing
2 Jan 2024	3:1 Dermacarrier, Model Number 00219501300, skin graft carrier	Device	Class II	1	Ongoing
5 Sep 2023	Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the dermatome handpiece which is a skin grafting instrument that is intended to provide variable graft thickness and width capabilities Part number: 00880000010	Device	Class II	1	Ongoing
3 Jan 2020	Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual Port, Dual Bladder, Item No. 60708015200, UDI (01)00889024377547 (17)230812(10)27968701 The product is a tourniquet - Product Usage: Tourniquets are intended to be used by qualified medical professionals to exert enough pressure on the…	Device	Class II	1	Terminated
16 Apr 2019	Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece, & Alvarado II Base Plate and Foot Piece: Alvarado Foot Piece: Item Number: 00-1320-010-00 Alvarado Knee Holder Base Plate Assembly: Item Number: 00-1320-011-00 Alvarado II Foot Piece: Item Number: 00-1320-210-00 Alvarado II Base Plate: Item…	Device	Class II	1	Terminated
8 Jun 2018	Zimmer Dermatone AN, Model No. 88710100	Device	Class II	1	Terminated
27 Jul 2017	A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily occlude blood flow in a patient's extremities during surgical procedures on those extremities. .	Device	Class II	2	Terminated
4 Jul 2016	Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a corrugated shipper carton or…	Device	Class II	1	Terminated
4 Jul 2016	Zimmer¿ Air Dermatome II Handpiece, item number 00-8851-001-00. The Zimmer Air Dermatome II handpiece and width plates are packaged inside of a padded-foam corrugate box. An operating manual is packed with the handpiece between the top foam pad and box lid. A product label is applied to the lid of the box. The width…	Device	Class II	7	Terminated
24 Jun 2015	18inch Dual Port/Single Bladder Disposable Tourniquet Cuff, Zimmer Surgical, Inc. Tourniquets are intended to be used by qualified medical professionals to exert enough pressure on the arterial blood flow in a limb to produce a bloodless operating field. Single bladder tourniquet cuffs are generally used for…	Device	Class II	2	Terminated
21 Apr 2015	Zimmer 100 mL Hemovac Device Hemovac Mini Evacuator. 00-2568-000-10. Zimmer Surgical, Inc. Intended for post-operative collection of wound drainage.	Device	Class III	1	Terminated
6 Oct 2014	UNIVERSAL Modular Electric/Battery Handpiece for surgery The electric handpiece is packaged within a foam bag inside of a padded-foam corrugate box. An operating manual is packed with the handpiece between the top foam pad and box lid. A product label is applied to the lid of the box. Product Usage: Surgical…	Device	Class II	1	Terminated
7 May 2013	The Zimmer Air Dermatome, REF 00- 8801- 001- 00 , Rx, non-sterile grafting instruments intended to provide variable graft thickness and width capabilities	Device	Class II	3	Terminated

By type and class

Device15

Class II14

Class III1

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for Zimmer Surgical Inc by year initiated.

Questions and answers

How many FDA recalls has Zimmer Surgical Inc had?

15 enforcement events (28 product records) on this register, 2013–2026: 15 device.

Are any Zimmer Surgical Inc recalls ongoing?

5 events are listed as ongoing in the current openFDA export.

What class are Zimmer Surgical Inc recalls?

14 Class II, 1 Class III. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.