In Re Sulzer Hip Prosthesis and Knee Prosthesis Liability Litigation

268 F. Supp. 2d 907, 2003 U.S. Dist. LEXIS 15662, 2003 WL 21456300
CourtDistrict Court, N.D. Ohio
DecidedJune 12, 2003
Docket1:01-CV-9000; MDL DOCKET NO. 1401
StatusPublished
Cited by20 cases

This text of 268 F. Supp. 2d 907 (In Re Sulzer Hip Prosthesis and Knee Prosthesis Liability Litigation) is published on Counsel Stack Legal Research, covering District Court, N.D. Ohio primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In Re Sulzer Hip Prosthesis and Knee Prosthesis Liability Litigation, 268 F. Supp. 2d 907, 2003 U.S. Dist. LEXIS 15662, 2003 WL 21456300 (N.D. Ohio 2003).

Opinion

MEMORANDUM AND ORDER

O’MALLEY, District Judge.

With this Order, the Court enters Attorney Fee Awards to certain attorneys in connection with their efforts to confer a Common Benefit to the Plaintiff Class in this Multi-District Litigation Class Action Settlement. The specific Fee Awards for each attorney are listed in the chart at the end of this Order.

As explained further below, the parties and the Court reserved a maximum of $50 million, out of a total settlement of over $1 billion, for the payment of Common Benefit Attorney Fee Awards. The total of the Fee Awards authorized by this Order is $30,232,300.00. In addition, the Court estimates it may authorize additional Fee Awards to certain attorneys in the amount of about $12,650,000.00, but the Court is withholding the entry of those awards at this time. 1 Assuming the Court’s estimate *910 of additional Fee Awards is accurate, this leaves a remainder of $7,117,700.00 (out of the $50 million reserve). The Court DIRECTS the Claims Administrator and the Trustee of the Sulzer Settlement Trust to continue to hold in reserve this entire $7,117,700.00 amount for payment of certain costs associated with effectuating the settlement and, if possible, distribution to the settlement class. 2

With regard to the specific, individual Fee Awards authorized by this Order, the Court further DIRECTS as follows. First, the Claims Administrator and the Trustee of the Sulzer Settlement Trust shall promptly COMPLY with sections 5.4 and 5.6 of the Settlement Agreement, which directs that these Fee Awards “shall be paid to liaison Class Counsel, who shall distribute such amounts to [the appropriate] Common Benefit Attorneys,” and states that the Fee Awards “shall be paid out of the [proceeds from the] CCI.”

Second, if an individual attorney desires an explanation of how the Court applied the relevant factors to reach its conclusion regarding his own common benefit fee award, the attorney must file a formal request therefor within ten calendar days of the date of this Order. The Court will then issue a brief written explanation, which will become an appendix to this Order. 3 The Court will provide a personal explanation only if requested by the attorney who actually submitted the common benefit Fee Application (or his law firm).

Except as noted in footnote 1 above, and pursuant to Fed.R.Civ.P. 58, this Order entering Fee Awards is a final appealable Order.

I. Background.

A. The Defective Products. 4

Sulzer Orthopedics, Inc. (“Sulzer Orthopedics”) is a Texas-based designer, *911 manufacturer, and distributor of orthopedic implants for hips, knees, shoulders, and elbows. During the relevant time-frame, Sulzer Orthopedics was wholly owned by Sulzer Medica USA Holding Company (“Sulzer Medica USA”), and Sulzer Medica USA was wholly owned by Sulzer Medica Ltd. (“Sulzer Medica”), a Swiss company. Sulzer AG, another Swiss company, owned 74% of Sulzer Medica. 5

One of the products manufactured by Sulzer Orthopedics is known as the “Inter-Op acetabular shell,” : mh is one component of a system used for complete hip replacements. Specifically, the Inter-Op shell is a socket-like device inserted into the acetabulum, which is a part of the pelvis; the shell is designed to receive a separate, ball-like device, which is inserted into the femur, or thigh bone. The two components thereby replace the articulating ball-and-socket structure of the hip joint. The Inter-Op shell is regulated by the federal Food and Drug Administration (“FDA”).

Proper surgical attachment of these replacement components in the body is critical. Orthopedic implants are often cemented or screwed into position. Some implants are also designed to allow the bone to grow into and around them, holding them securely in place. The Inter-Op acetabular shell was designed to bond with the natural bone.

Unfortunately, a manufacturing defect apparently prevented some of Sulzer Orthopedics’ Inter-Op shells from bonding with the acetabulum. In early December of 2000, Sulzer Orthopedics announced a voluntary recall of certain manufacturing lots of its Inter-Op shells. Most of the recalled products were manufactured during or after October of 1999, but a limited number were produced as early as June of 1997. The recall stated that Sulzer Orthopedics had “received reports of post-operative loosening” of some of the Inter-Op shells, apparently “related to a reaction of the [human] body to a slight residue of lubricant used in the manufacturing process.” Sulzer Orthopedics recalled approximately 40,000 units of its Inter-Op shell, of which about 26,000 had already been implanted in patients. About 90% of these implants occurred in the United States. With regard to the recalled units, Sulzer Orthopedics “reprocessed” some of them — that is, “re-cleaned” about 16,500 of the never-implanted, recalled shells — and then resold them. About 6,100 of these reprocessed units were implanted.

One of the documents issued by Sulzer Orthopedics in connection with the voluntary recall included the following explanation:

Sulzer Orthopedics is the manufacturer of a hip implant that you received during hip replacement surgery. We sincerely regret to inform you that we have recently learned that a small number of the many implant parts that we manufactured may have a trace of lubricant residue on the surface that was not completely removed during the manufacturing process.
% iH % # ‡ %
*912 The hip implant part is the acetabular “shell” which was implanted into the upper part of your hip called the aceta-bulum. Normally, the bone would form an integrated bond with the shell; however, it appears that bone does not always bond with shells when the lubricant residue is present. Reported symptoms include severe groin pain and inability to bear weight on your leg. These symptoms are caused by the shell being loose from the bone. Only a small number of patients who received the shell during their total hip replacement have experienced loosening of the shell.

In fact, to date, over 3,800 of the patients who received implants of the defective Inter-Op shells have undergone “revision surgery” — removal of the defective implant and replacement with a new one. 6 For a variety of reasons, not all of the patients who were implanted with recalled Inter-Op shells will undergo revision surgery. For example, some patients will not experience any bone-bonding failure; other patients may suffer severe failure but be medically ineligible for revision surgery.

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Bluebook (online)
268 F. Supp. 2d 907, 2003 U.S. Dist. LEXIS 15662, 2003 WL 21456300, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-sulzer-hip-prosthesis-and-knee-prosthesis-liability-litigation-ohnd-2003.