RecallHawk
Class II Recall

NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Porous Femur System.

Zimmer, Inc.

Summary

The FDA issued a Class II for NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the by Zimmer, Inc.. Reason: Out of specification violation of devices that results in a gap existing within the fixture that presses the fiber metal pad to the substrate, causing.

Details

Source

Device Recall

External ID

Z-1608-2024

Action Date

2024-05-01

Status

Ongoing

Category

device

Product Description

NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Porous Femur System.

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(01)00889024207806(17)331107(10)66324859, (01)00889024207790(17)331111(10)66324849, (01)00889024207790(17)331126(10)66324846, (01)00889024207806(17)331127(10)66324856, (01)00889024207790(17)331201(10)66324852, (01)00889024207806(17)331203(10)66324862, (01)00889024207790(17)331208(10)66378806, (01)00889024207790(17)331212(10)66364015, (01)00889024207820(17)340110(10)66378834, (01)00889024207806(17)340113(10)66364020; Lot Code: 64115713, 64175075, 64175076, 64175073, 64138317, 64175074, 64194991, 64202116, 64178998, 64179054, 64202117, 64179043, 64194989, 64178996, 64178997, 64179023, 64178999, 64179043R, 64194989R, 64202115, 64226003, 64226007, 64226008, 64220651, 64226001, 64226006, 64202119, 64226002, 64202118, 64254389, 64254390, 64226077, 64226078, 64226009, 64226076, 64254387, 64254388, 64261032, 64226129, 64242244, 64254386, 64226076R, 64254386R, 64254387R, 64261030, 64275592, 64275434, 64261033, 64261035, 64261031, 64275593, 64261029, 64275538, 64275540, 64261037, 64261036, 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65521956, 65559114, 65559112, 65573605, 65573604, 65602373, 65594083, 65602376, 65611118, 65696513, 65617532, 65625154, 65751453, 65738055, 66005557, 66005559, 11025242, 66005554, 66324843, 66324859, 66324849, 66324846, 66324856, 66324852, 66324862, 66378806, 66364015, 66378834, 66364020.

Quantity Affected: 5,546 units

Reason for Recall

Out of specification violation of devices that results in a gap existing within the fixture that presses the fiber metal pad to the substrate, causing the pad to not fully bond to the substrate.

Distribution

Worldwide distribution - US Nationwide including the states of AK, AL, CA, FL, GA, IL, IN, KS, KY, MA, MD, ME, MI, MN, MO, NC, NH, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI and the countries of Australia, Canada, Japan, Netherlands.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-28

Company

Zimmer, Inc.

Warsaw, IN

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 203 device recalls issued in the same week, part of 403 device-related FDA actions this month.

Zimmer, Inc. has 87 FDA actions in our database, including 65 recalls and 22 clearances.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Zimmer, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Zimmer, Inc. have FDA actions?

Zimmer, Inc. has 87 FDA actions in our database, including 65 recalls and 22 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "Z-1608-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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