Stanmore Implants Worldwide recalls

Stanmore Implants Worldwide has 8 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 13 Sep 2017. The most frequent reason is packaging defects.

Total recalls8since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 13 Sep 2017

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 8 100%Class III 0 0%

Why stanmore implants worldwide is recalled

Product types

Hip & Knee Implants8100%

By year

2017113%
2016788%

All stanmore implants worldwide recalls, newest first

8 total

Reported	Class	Recall	Company	Reason	Where
13 Sep 2017Device	CLASS II	JTS External Drive Unit JTS Distal Femoral Extendible recalled	Stanmore Implants Worldwide	Other	10 states
28 Dec 2016Device	CLASS II	Tibial Component Metal Cased Small Long recalled	Stanmore Implants Worldwide	Foreign Material	Nationwide
28 Dec 2016Device	CLASS II	Femoral Shaft L=; Femoral Shaft L= recalled	Stanmore Implants Worldwide	Packaging Defects	Nationwide
28 Dec 2016Device	CLASS II	DF Coated Integral Shaft & Stem 15x30x38 recalled	Stanmore Implants Worldwide	Packaging Defects	Nationwide
28 Dec 2016Device	CLASS II	Femoral Integral Shaft & Stem HA Coated recalled	Stanmore Implants Worldwide	Packaging Defects	Nationwide
28 Dec 2016Device	CLASS II	Tibial Component Fixed Hinge Small Long recalled	Stanmore Implants Worldwide	Packaging Defects	Nationwide
24 Aug 2016Device	CLASS II	Mets Smiles Total Knee Replacement recalled	Stanmore Implants Worldwide	Device Malfunction	AL, MS, TX
18 May 2016Device	CLASS II	Distal Femoral Replacement (patient specific recalled	Stanmore Implants Worldwide	Other	OH

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.