Product 44 consists of all product under
Medical device recall Z-1142-2016. Published in FDA’s Enforcement Report on Mar 23, 2016.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Mar 23, 2016. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 4335 how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is 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.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
As a result of the insufficient sealer calibration data for product packaged in firm’s Building II between August 2010 and April 2013. The affected products are sterile.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Product 44 consists of all product under product code: HWC and same usage: Item no: 114607099 MAGMA-FX CANN SCREW 7.0MM 114604099 MAGNA FX CANN SCREW 7.0MM 114603000 MAGNA-FX CANN SCREW 7.0MM 114603500 MAGNA-FX CANN SCREW 7.0MM 114604000 MAGNA-FX CANN SCREW 7.0MM 114604032 MAGNA-FX CANN SCREW 7.0MM 114604500 MAGNA-FX CANN SCREW 7.0MM 114604532 MAGNA-FX CANN SCREW 7.0MM 114604599 MAGNA-FX CANN SCREW 7.0MM 114605000 MAGNA-FX CANN SCREW 7.0MM 114605032 MAGNA-FX CANN SCREW 7.0MM 114605099 MAGNA-FX CANN SCREW 7.0MM 114605500 MAGNA-FX CANN SCREW 7.0MM 114605532 MAGNA-FX CANN SCREW 7.0MM 114605599 MAGNA-FX CANN SCREW 7.0MM 114606000 MAGNA-FX CANN SCREW 7.0MM 114606032 MAGNA-FX CANN SCREW 7.0MM 114606099 MAGNA-FX CANN SCREW 7.0MM 114606500 MAGNA-FX CANN SCREW 7.0MM 114606532 MAGNA-FX CANN SCREW 7.0MM 114606599 MAGNA-FX CANN SCREW 7.0MM 114607000 MAGNA-FX CANN SCREW 7.0MM 114607032 MAGNA-FX CANN SCREW 7.0MM 114607500 MAGNA-FX CANN SCREW 7.0MM 114607532 MAGNA-FX CANN SCREW 7.0MM 114607599 MAGNA-FX CANN SCREW 7.0MM 114608000 MAGNA-FX CANN SCREW 7.0MM 114608032 MAGNA-FX CANN SCREW 7.0MM 114608099 MAGNA-FX CANN SCREW 7.0MM 114608500 MAGNA-FX CANN SCREW 7.0MM 114608532 MAGNA-FX CANN SCREW 7.0MM 114608599 MAGNA-FX CANN SCREW 7.0MM 114609000 MAGNA-FX CANN SCREW 7.0MM 114609032 MAGNA-FX CANN SCREW 7.0MM 114609099 MAGNA-FX CANN SCREW 7.0MM 114609500 MAGNA-FX CANN SCREW 7.0MM 114609532 MAGNA-FX CANN SCREW 7.0MM 114609599 MAGNA-FX CANN SCREW 7.0MM 114610000 MAGNA-FX CANN SCREW 7.0MM 114610032 MAGNA-FX CANN SCREW 7.0MM 114610099 MAGNA-FX CANN SCREW 7.0MM 114610500 MAGNA-FX CANN SCREW 7.0MM 114610532 MAGNA-FX CANN SCREW 7.0MM 114610599 MAGNA-FX CANN SCREW 7.0MM 114611000 MAGNA-FX CANN SCREW 7.0MM 114611032 MAGNA-FX CANN SCREW 7.0MM 114611099 MAGNA-FX CANN SCREW 7.0MM 114611500 MAGNA-FX CANN SCREW 7.0MM 114611532 MAGNA-FX CANN SCREW 7.0MM 114611599 MAGNA-FX CANN SCREW 7.0MM 114612000 MAGNA-FX CANN SCREW 7.0MM 114612032 MAGNA-FX CANN SCREW 7.0MM 114612500 MAGNA-FX CANN SCREW 7.0MM 114612599 MAGNA-FX CANN SCREW 7.0MM 114613000 MAGNA-FX CANN SCREW 7.0MM 114613099 MAGNA-FX CANN SCREW 7.0MM 511007020 MGII KNEE SLF-TAP BONE ST 511007025 MGII KNEE SLF-TAP BONE ST 511007030 MGII KNEE SLF-TAP BONE ST 511007035 MGII KNEE SLF-TAP BONE ST 511007040 MGII KNEE SLF-TAP BONE ST 511007045 MGII KNEE SLF-TAP BONE ST 114204012 MINI MAGNA-FX CANN SCREW 114204016 MINI MAGNA-FX CANN SCREW 114204020 MINI MAGNA-FX CANN SCREW 114204024 MINI MAGNA-FX CANN SCREW 114204028 MINI MAGNA-FX CANN SCREW 114204032 MINI MAGNA-FX CANN SCREW 114204036 MINI MAGNA-FX CANN SCREW 114204040 MINI MAGNA-FX CANN SCREW 114204044 MINI MAGNA-FX CANN SCREW 114204048 MINI MAGNA-FX CANN SCREW 114204055 MINI MAGNA-FX CANN SCREW 114204065 MINI MAGNA-FX CANN SCREW 114204124 MINI MAGNA-FX CANN SCREW 114204126 MINI MAGNA-FX CANN SCREW 114204128 MINI MAGNA-FX CANN SCREW 114204130 MINI MAGNA-FX CANN SCREW 114204132 MINI MAGNA-FX CANN SCREW 114204134 MINI MAGNA-FX CANN SCREW 114204136 MINI MAGNA-FX CANN SCREW 114204138 MINI MAGNA-FX CANN SCREW 114204140 MINI MAGNA-FX CANN SCREW 114204142 MINI MAGNA-FX CANN SCREW 114204144 MINI MAGNA-FX CANN SCREW 114204146 MINI MAGNA-FX CANN SCREW 114204148 MINI MAGNA-FX CANN SCREW 114204150 MINI MAGNA-FX CANN SCREW 114204155 MINI MAGNA-FX CANN SCREW 114204160 MINI MAGNA-FX CANN SCREW 114204165 MINI MAGNA-FX CANN SCREW 114204170 MINI MAGNA-FX CANN SCREW 114205012 MINI MAGNA-FX CANN SCREW 114205016 MINI MAGNA-FX CANN SCREW 114205020 MINI MAGNA-FX CANN SCREW 114205024 MINI MAGNA-FX CANN SCREW 114205028 MINI MAGNA-FX CANN SCREW 114205032 MINI MAGNA-FX CANN SCREW 114205036 MINI MAGNA-FX CANN SCREW 114205040 MINI MAGNA-FX CANN SCREW 114205044 MINI MAGNA-FX CANN SCREW 114205048 MINI MAGNA-FX CANN SCREW 114205055 MINI MAGNA-FX CANN SCREW 114205065 MINI MAGNA-FX CANN SCREW 114205124 MINI MAGNA-FX CANN SCREW 114205126 MINI MAGNA-FX CANN SCREW 114205128 MINI MAGNA-FX CANN SCREW
4335, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
lot no.: 61740618 61740619 61931831 61920071 62221457 61825071 61926436 62036483 62221458 61758528 61820880 61878510 62098534 62221459 61851882 61986815 61825053 61851890 61926437 62094921 62181573 62221461 61878509 62098535 62181574…
Every code shown here, 1,998 characters
lot no.: 61740618 61740619 61931831 61920071 62221457 61825071 61926436 62036483 62221458 61758528 61820880 61878510 62098534 62221459 61851882 61986815 61825053 61851890 61926437 62094921 62181573 62221461 61878509 62098535 62181574 61758529 61828387 61851894 61915518 61979050 62065546 62065954 62160485 62221462 62253412 61878508 61979052 62181575 62253417 61930994 61812109 61812110 61857821 61898941 61898944 62065556 62065966 62160486 62225720 61830574 61926438 62112852 62253418 62181576 61758530 61798087 61831417 61851896 61920073 61920076 61979053 61986817 62191389 62260412 61627280 61758593 61851898 61920080 61979057 62098542 62191391 62260435 61740613 61620151 61740615 61758597 61814991 61851906 61851908 61857822 61920081 61964951 61964953 61979058 62098544 62191387 62225721 61825064 61851910 61918613 61964954 62036488 62120735 62181577 62260456 62160478 61627282 61740616 61758600 61825051 61825052 61851911 61851913 61915519 61979059 61979060 62094922 62094923 62122194 62181545 62181546 62210926 62210928 62265689 62265690 61678540 61758601 61851912 61926442 62036492 62112496 62204454 61678541 61758603 61758605 61798068 61825059 61835206 61844448 61844451 61851918 61898975 61898978 61964957 61964960 61979062 62065551 62065961 62120742 62144846 62204457 62204458 62204460 61835208 61920082 61979063 62094924 62120743 62253422 62141639 61740623 61740625 61758611 61820859 61825063 61830556 61844453 61844454 61851926 61857823 61915364 61915365 61915366 61964962 61964963 61986818 61986819 62065542 62065944 62098546 62112497 62112498 62112499 62160487 62181578 62204470 62204474 62204478 62204481 61758631 61825125 61851930 61964458 62031594 62144847 62225722 61812106 62141640 61740632 61752977 61810352 61825057 61830554 61835211 61851932 61851935 61851939 61878511 61898980 61915520 61964964 61964965 61986820 62026967 62094925 62101351 62101359 62122193 62140571 62140572 62204488 62204489 62204491 62204492 61664696 61812125 61812127 61812128 61920083 61986824 62101364…
FDA’s list runs to 3,176 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
US Nationwide Distribution
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Jan 11, 2016.
- FDA classified it on Mar 12, 2016.
- FDA’s Enforcement Report published it on Mar 23, 2016.
- FDA terminated it on Apr 13, 2017.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Zimmer Manufacturing B.V., of Mercedita, PR.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 3,176 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.