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Implants & Prosthetics

🏥 Medical Devices 4,540 recalls

The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.

Nov 29, 2017 Implants & Prosthetics Nationwide View Details →

The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.

Nov 29, 2017 Implants & Prosthetics Nationwide View Details →

The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.

Nov 29, 2017 Implants & Prosthetics Nationwide View Details →

The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.

Nov 29, 2017 Implants & Prosthetics Nationwide View Details →

The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.

Nov 29, 2017 Implants & Prosthetics Nationwide View Details →

The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.

Nov 29, 2017 Implants & Prosthetics Nationwide View Details →

The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.

Nov 29, 2017 Implants & Prosthetics Nationwide View Details →

Medtronic implemented a final design change intended to address the motor stall due to corrosion and is recalling devices with the previous design that are not implanted.

Aug 9, 2017 Implants & Prosthetics Nationwide View Details →

The complaints database was reviewed and there have been an atypical volume of dull blades complaints for various lots. out of an abundance of precaution, Bausch + Lomb is voluntarily recalling all product codes SKU manufacturing without the electro-polish control and penetration force testing.

Mar 3, 2017 Implants & Prosthetics Nationwide View Details →

The complaints database was reviewed and there have been an atypical volume of dull blades complaints for various lots. out of an abundance of precaution, Bausch + Lomb is voluntarily recalling all product codes SKU manufacturing without the electro-polish control and penetration force testing.

Mar 3, 2017 Implants & Prosthetics Nationwide View Details →