Device recall: Zimmer M/L Taper Hip Prosthesis Plasma Sprayed, Size 4 Extended Offset, 00-7711-004-40

Class II FDA enforcement event 80188. Recall start date: 30 May 2018. Status in the FDA record: Terminated. Termination date: 28 May 2020.

Reason for recall, in the words of FDA

M/L Taper Hip Prosthesis and M/L Taper Hip Prosthesis with Kinectiv Technology manufactured prior to October 2015 are being recalled due to the potential for black residue to be observed within the polyethylene bag containing the implant. The black residue is a combination of the titanium plasma spray used to create the porous surface of the implant and polyethylene bag containing the implant.…

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

Zimmer Biomet, Inc. started this device recall on 30 May 2018. The firm address in the FDA record is in Warsaw, IN. FDA put the recall in Class II. FDA event 80188 has 15 product records. The first FDA enforcement report date is 11 Jul 2018. The record gives the status Terminated, with the termination date 28 May 2020.

FDA enforcement report The 15 product records

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on 1 Oct 2026. openFDA export of 28 Sep 2026.

Distribution

In the words of FDA.

Products were distributed solely to Japan.

Recalling firm

Zimmer Biomet, Inc., Warsaw, IN.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

15 product records in the event.

FDA event 80188: product records
Recall number	Product	Quantity	Class	Status	Report date
Z-2361-2018	Zimmer M/L Taper Hip Prosthesis Plasma Sprayed, Size 4 Extended Offset, 00-7711-004-40	280	Class II	Terminated	11 Jul 2018
Z-2362-2018	Zimmer M/L Taper Hip Prosthesis Plasma Sprayed, Size 4 Standard Offset; 00-7711-004-10	294	Class II	Terminated	11 Jul 2018
Z-2363-2018	Zimmer M/L Taper Hip Prosthesis With Kinectiv Technology Cementless, Size 5; 00-7713-005-00	227	Class II	Terminated	11 Jul 2018
Z-2364-2018	Zimmer M/L Taper Hip Prosthesis With Kinectiv Technology Cementless, Size 6; 00-7713-006-00	96	Class II	Terminated	11 Jul 2018
Z-2365-2018	Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 10; 00-7713-010-00	24	Class II	Terminated	11 Jul 2018
Z-2366-2018	Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 11; 00-7713-011-00	132	Class II	Terminated	11 Jul 2018
Z-2367-2018	Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 12.5; 00-7713-012-00	84	Class II	Terminated	11 Jul 2018
Z-2368-2018	Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 13.5; 00-7713-013-00	510	Class II	Terminated	11 Jul 2018
Z-2369-2018	Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 15; 00-7713-015-00	1024	Class II	Terminated	11 Jul 2018
Z-2370-2018	Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 16.25; 00-7713-016-00	665	Class II	Terminated	11 Jul 2018
Z-2371-2018	Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 17.5; 00-7713-017-00	182	Class II	Terminated	11 Jul 2018
Z-2372-2018	Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 20; 00-7713-020-00	138	Class II	Terminated	11 Jul 2018
Z-2373-2018	Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 22.5; 00-7713-022-00	101	Class II	Terminated	11 Jul 2018
Z-2374-2018	Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 7.5; 00-7713-007-00	58	Class II	Terminated	11 Jul 2018
Z-2375-2018	Zimmer M/L Taper Hip Prosthesis With Kinective Technology Cementless, Size 9; 00-7713-009-00	116	Class II	Terminated	11 Jul 2018

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2018: 1,074
Share of these events in Class II: 92%
Product records in this event: 15Median of the firm: 1
Events of the firm on the register: 144

Other events of the firm

Other FDA enforcement events of Zimmer Biomet, Inc.
Initiated	Product (first record)	Type	Class	Records
20 Nov 2020	Spinal Rod Cutter, Item number 00392500200. The product is a nonsterile pin cutter - Product Usage: The intended use of	Device	Class II	1
17 Nov 2020	Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system	Device	Class II	1
24 Sep 2020	ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, Neutral, O.D. Cup with Spacers, 43mm Item Nu	Device	Class II	75
14 Aug 2020	Dual Mobility Vivacit-E Bearing, Model Number 110031009	Device	Class II	1
5 May 2020	Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 4.5X30MM, Item Number 810M4530 - Product Usage: are non-cerv	Device	Class II	25
7 Jan 2020	THP Hip Plating System, Item Nos. 14-451070 14-451075 14-451080 14-451085 14-451090 14-451095 14-451100 14-451105 14-451	Device	Class II	1
23 Dec 2019	Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00	Device	Class II	1
19 Dec 2019	ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Mode Number: 110032332 Product Usage: The device is a general orth	Device	Class II	1
12 Dec 2019	Coonrad/Morrey Total Elbow Humeral Assembly, Extra Small, 4-inch Length. Model No. 32-8105-027-04. UDI (01)0088902427400	Device	Class II	1
25 Oct 2019	Biomet Orthopedics Intramedullary Bone Saw Cam Assembly 13MM-Orthopedic manual surgical instrument Item Number: 475660	Device	Class II	2

Zimmer Biomet, Inc.: all 144 events

Official channels

FDA enforcement report Z-2361-2018The FDA record of the first product of this event.
FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
FDA MedWatchThe FDA safety reporting program for drugs and medical devices.

Follow by RSS:Food, drug and device recallsFDA Class I recalls

Cite this page

Recall Register. FDA enforcement event 80188. https://recallregister.com/fda/ii/80188/. Source: openFDA enforcement reports. Data through 28 Sep 2026.

Sources

Source: openFDA device enforcement reports
Licence: CC0 1.0
Export date: 28 Sep 2026
Newest FDA report date on the register: 23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?: The FDA record gives this distribution: Products were distributed solely to Japan.
What quantity of product is in FDA event 80188?: The event has 15 product records. The first record gives this quantity: 280
How did the recall start?: The FDA record says: Voluntary: Firm initiated
How many device recalls of 2018 have the same class?: 92% of the 1,074 device events that started in 2018 are in Class II.