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

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    LOTS: 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 204970 204990 205000 205010 205020 472130 164579 164582 164586 164587 206318 206319 206320 206321 260820 260821 270166 270167 AF6AE7000 AT9AG7 B5KAT7 B5LAA7 B78AE7 B78AF7 BD3AA7 BT9AD7 BX2AB7 CN8AG7 CN8AH7 CW3AT7 CW3AV7 CW3AV7R CW3AW7 CW3AW7R CW3AX7 E3SAB7 E3SAC7 EG9AF7 EG9AG7 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
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Zimmer Biomet, Inc.
Reason for Recall:
Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

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

Product Codes/Lot Numbers:

LOTS: 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 204970 204990 205000 205010 205020 472130 164579 164582 164586 164587 206318 206319 206320 206321 260820 260821 270166 270167 AF6AE7000 AT9AG7 B5KAT7 B5LAA7 B78AE7 B78AF7 BD3AA7 BT9AD7 BX2AB7 CN8AG7 CN8AH7 CW3AT7 CW3AV7 CW3AV7R CW3AW7 CW3AW7R CW3AX7 E3SAB7 E3SAC7 EG9AF7 EG9AG7 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

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0531-2020

Related Recalls

Zimmer Biomet is conducting a medical device correction to update the Instructions for Use (IFU) and the Surgical Techniques for the Polaris Spinal System Translation Screw and Cypher MIS Screw System. Users should be aware that changes were made to the contraindications section indicating that the Translation Screws should not be used with a direct current stimulation, as a high probability of construct failure exists when using Translation Screws containing CoCr with direct current simulation system.

Nov 17, 2020 Other Medical Devices Nationwide View Details →