Z-1132-2015Class II

CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for...

Name: Z-1132-2015 CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for...
Creator: Zimmer Gmbh
Published: 2014-12-17
License: https://open.fda.gov/license/

Zimmer GmbH / initiated 2014-12-17 / Terminated / root cause: packaging

FDA source

Zimmer Gmbh began a recall of CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of the proximal femur in total hip... on 2014-12-17. FDA classified it as Class II and gives the reason as "Potential compromise of the inner sterile tray. If a compromised tray is detected, a delay in surgery may result. If undetected breach in both the inner and outer trays were to occur, and there is contamination present...". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-1132-2015
Classification: Class II
Status: Terminated
Initiated: 2014-12-17
Posted: 2015-02-20
Terminated: 2015-09-23
Recalling firm: Zimmer GmbH
Product: CoCr Femoral Head - A modular head component is used in conjunction with a femoral stem component for replacement of the proximal femur in total hip arthroplasty.
Product code: LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Reason for recall: Potential compromise of the inner sterile tray. If a compromised tray is detected, a delay in surgery may result. If undetected breach in both the inner and outer trays were to occur, and there is contamination present, a periprosthetic infection is possible, which could lead to revision.
Root cause tag: packaging
FDA root cause: Package design/selection
Action: On 12/17/2014, URGENT MEDICAL DEVICE RECALL notifications were sent to the affected distributors and hospital Risk Managers with instructions for returning the affected product. All distributors were notified via electronic mail, and all hospital Risk Managers and distributors with affected inventory were also notified via courier. The recall notification included a description of the reason for the recall, affected product, consignee responsibilities, and instructions for responding to the formal recall notification. For questions, call the customer call center at 1-800-348-2759.
Quantity in commerce: 1908
Distribution: Domestic: AK, AL, AR, AZ, CA, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MS, MA, MD, ME, MI, MN, MO, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY International: Canada, Japan
Product codes and lots: Item numbers: 01.01012.384; 01.01012.385; 01.01012.386; 01.01012.387; 01.01012.388; 01.01012.444; 01.01012.445; 01.01012.446; 01.01012.447; 01.01012.448 Lot #'s: 2551762, 2542690, 2542691, 2543993, 2544892, 2544893, 2551930, 2551931, 2557054, 2558475, 2559787, 2563363, 2564657, 2568082, 2539887, 2540911, 2544894, 2544895, 2545830, 2545831, 2545832, 2545833, 2547043, 2547807, 2548952, 2551330, 2551860, 2551861, 2554798, 2554799, 2554800, 2558476, 2558477, 2559788, 2561617, 2562662, 2563364, 2563385, 2565407, 2566564, 2567294, 2542692, 2542693, 2544896, 2547044, 2548953, 2551932, 2553210, 2556029, 2559603, 2563386, 2539888, 2540926, 2548954, 2553419, 61487633, 61487634, 61636015, 61495961, 61495962, 61495963, 61562431, 61577697, 61608436, 61562432, 61577709, 61487635, 61562448

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1132-2015
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1132-2015	Class II	Terminated	Voluntary: Firm initiated	2015-03-04	2015-02-20
Z-1133-2015	Class II	Terminated	Voluntary: Firm initiated	2015-03-04	2015-02-20
Z-1134-2015	Class II	Terminated	Voluntary: Firm initiated	2015-03-04	2015-02-20
Z-1135-2105	Class II	Terminated	Voluntary: Firm initiated	2015-03-04	2015-02-20
Z-1136-2015	Class II	Terminated	Voluntary: Firm initiated	2015-03-04	2015-02-20

Product code LPH

K993259Class IIInter-Op Durasul Acetabular Inserts/cocr Femoral HeadsSulzer Orthopedics, Inc. / cleared 2000-03-10

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-14, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)