Reported Dec 4, 2019 · Terminated

2.0MM BALL NOSE GUIDE WIRE, Item Nos. 281017006 - Product Usage: These instruments and delivery systems are used to…

Zimmer Biomet, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Zimmer Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989

Is this the product you have?

- 2.0MM BALL NOSE GUIDE WIRE
- Item Nos. 281017006 -
Product UsageThese instruments and delivery systems are used to facilitate implantation of orthopedic medical devices

Lot codes and dates: LOTS
99 of 99 codes
206322
062980
062690
062720
062740
062760
062950
062960
062970
730390
730400
730380
158530
158510
158520
460220
859610
860250
661640
977840
977850
114600
167450
204150
204160
204180
204190
204200
204210
678430
491410
678420
233730
233770
392590
233710
233720
694090
039330
039340
039350
039360
039370
039380
039450
039420
039390
039400
039410
039430
039440
039460
039470
113340
994740
036320
036330
665740
994730
036290
EG9AH7 EG9AJ7 NXW351U NXW351V UDI(01)00887868029448(17)220501(10)206322 (01)00887868029448(17)240819(10)062980 (01)00887868029448(17)240819(10)062690 (01)00887868029448(17)240819(10)062720 (01)00887868029448(17)240819(10)062740 (01)00887868029448(17)240819(10)062760 (01)00887868029448(17)240819(10)062950 (01)00887868029448(17)240819(10)062960 (01)00887868029448(17)240819(10)062970 (01)00887868029448(17)241013(10)730390 (01)00887868029448(17)241013(10)730400 (01)00887868029448(17)241013(10)730380 (01)00887868029448(17)241101(10)158530 (01)00887868029448(17)241103(10)158510 (01)00887868029448(17)241103(10)158520 (01)00887868029448(17)241201(10)460220 (01)00887868029448(17)250115(10)859610 (01)00887868029448(17)250116(10)860250 (01)00887868029448(17)250410(10)661640 (01)00887868029448(17)250429(10)977840 (01)00887868029448(17)250429(10)977850 (01)00887868029448(17)250601(10)114600 (01)00887868029448(17)250601(10)167450 (01)00887868029448(17)250921(10)204150 (01)00887868029448(17)250921(10)204160 (01)00887868029448(17)250921(10)204180 (01)00887868029448(17)250921(10)204190 (01)00887868029448(17)250922(10)204200 (01)00887868029448(17)250922(10)204210 (01)00887868029448(17)260614(10)678430 (01)00887868029448(17)260623(10)491410 (01)00887868029448(17)260108(10)678420 (01)00887868029448(17)260111(10)233730 (01)00887868029448(17)260111(10)233770 (01)00887868029448(17)260616(10)392590 (01)00887868029448(17)260111(10)233710 (01)00887868029448(17)260111(10)233720 (01)00887868029448(17)260403(10)694090 (01)00887868029448(17)260502(10)039330 (01)00887868029448(17)260502(10)039340 (01)00887868029448(17)260502(10)039350 (01)00887868029448(17)260502(10)039360 (01)00887868029448(17)260505(10)039370 (01)00887868029448(17)260505(10)039380 (01)00887868029448(17)260524(10)039450 (01)00887868029448(17)260525(10)039420 (01)00887868029448(17)260525(10)039390 (01)00887868029448(17)260525(10)039400 (01)00887868029448(17)260525(10)039410 (01)00887868029448(17)260525(10)039430 (01)00887868029448(17)260525(10)039440 (01)00887868029448(17)260525(10)039460 (01)00887868029448(17)260525(10)039470 (01)00887868029448(17)260610(10)113340 (01)00887868029448(17)260610(10)994740 (01)00887868029448(17)260623(10)036320 (01)00887868029448(17)260623(10)036330 (01)00887868029448(17)260623(10)665740 (01)00887868029448(17)260623(10)994730 (01)00887868029448(17)260701(10)036290 (01)00887868029448(17)260718(10)204970 (01)00887868029448(17)260718(10)204990 (01)00887868029448(17)260718(10)205000 (01)00887868029448(17)260718(10)205010 (01)00887868029448(17)260718(10)205020
Amount recalled: 2708

This recall covers 16 products

The agency filed one notice per product. You are reading one of them; the other 15 are below.

3 more are in the archive.

Where it was sold

Nationwide

Why it was recalled

Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Zimmer Biomet, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.

By hazard

Medical device recalls

Other recalls from Zimmer Biomet, Inc.

84 in total.

All recall categories · Browse the whole archive