🏥 Medical Devices Class I - Dangerous
For soft tissue fixation
All Recalls
95,075 total recalls in our database
🏥 Medical Devices Class I - Dangerous
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.
🏥 Medical Devices Class I - Dangerous
Medimop is recalling certain lots of this product Vial2Bag DC due to the potential of the IV Port separating from the Via12Bag DC body during the drug reconstitution I IV Set attachment process.
🏥 Medical Devices Class I - Dangerous
Label does not state that the product is heparin-coated.
🏥 Medical Devices Class I - Dangerous
Contact lenses lack sterility assurance.
IMRIS ORT100 Table, Part Number 110470-000
Deerfield Imaging
🏥 Medical Devices Class I - Dangerous
The rotational locking mechanisms on the ORT 100/ T2X tables can become disengaged or unlocked while in use which could potentially result in unintended movement of the table.
CPT 12/14 COCR SIZE 2 STD prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Zimmer Biomet
🏥 Medical Devices Class I - Dangerous
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.
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.
🏥 Medical Devices Class I - Dangerous
Two lots of hip implants are mislabeled.
CPT 12/14 COCR SIZE 1 EXT prosthesis, hip, semi-constrained, metal/polymer, porous uncemented
Zimmer Biomet
🏥 Medical Devices Class I - Dangerous
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.
🏥 Medical Devices Class I - Dangerous
HighPuragar was mislabeled and inadvertently sold as Noble Agar.
Proteus 235, Proton Therapy System a medical device designed to produce and delivers a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.
Ion Beam Applications S.A.
🏥 Medical Devices Class I - Dangerous
There is a risk of misalignment of the patient when using treatment plans with multiple isocenters.
Immunoassay Premium Plus Controls (3x4x5mL and 12x5mL packages)
Randox Laboratories
🏥 Medical Devices Class I - Dangerous
The ACTH in Immunoassay Premium and Premium Plus quality control does not meet the quoted reconstituted stability claim in the product IFU.
Newton Wire Guide
Cook
🏥 Medical Devices Class I - Dangerous
Label does not state that the product is heparin-coated.
🏥 Medical Devices Class I - Dangerous
Contact lenses lack sterility assurance.
Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
🏥 Medical Devices Class I - Dangerous
An accessory (range shifter, ridge filter&) can be improperly inserted in snout 300x400 with one rail only and the proton therapy system can still operate.
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.
🏥 Medical Devices Class I - Dangerous
Product may contain the presence of melted sterile packaging upon opening.
🏥 Medical Devices Class I - Dangerous
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.