Smith & Nephew, Inc. recalls 6.5MMX165MM CANNULATED SCREW
The product label incorrectly indicated that the screws are fully threaded, but the screws contained in the package were partially threaded.
Read the official notice →- Date
- 2021-10-27
- Country
- United States
- Brand
- Smith & Nephew
- Product
- 6.5MMX165MM CANNULATED SCREW
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide distribution in the states of OK, TN…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Smith & Nephew recalls
- 2022-07-27
US
Smith & Nephew, Inc. recalls (1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186. (2) Genesis II Non-Porous Tibial Baseplate Size 4 Left,…
The product was mispackaged (swapped). The devices within the inner tray matches the inner tray but does not match the outer box label and the chart sticks.
FDA · DeviceSmith & Nephew, Inc.US Nationwide distribution in the states of AZ, CA, GA, KS, LA, MN, MI, MO,…Official notice →- 2022-05-25
US
Smith & Nephew Inc recalls LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5
It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box labelled as a LEGION NARROW PS OXIN SZ 6N RT.
FDA · DeviceSmith & Nephew IncWorldwide distribution - US Nationwide distribution in the states of CT, NC,…Official notice →- 2022-02-16
US
Smith & Nephew, Inc. recalls Acufex Access Advanced Positioning Kit - indicated for use to position and distract the extremity of patient during open and arthroscopic…
Products were shipped to the Global Distribution Center instead of the sterilizer and therefore product did not undergo the sterilization process
FDA · DeviceSmith & Nephew, Inc.Worldwide distribution - US Nationwide distribution in the states of CO, CT,…Official notice →- 2022-02-09
US
Smith & Nephew, Inc. recalls INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND
The affected screwdrivers are out of specification and may not mate with the Surfix Alpha Lock screw
FDA · DeviceSmith & Nephew, Inc.US Nationwide distribution in the states of CA and OH.Official notice →- 2021-12-22
US
Smith & Nephew, Inc. recalls smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE, L, 5H, 90MM, REF 72573101
Testing vendor notified Smith & Nephew that previous MRI scanning conditions provided in Exponents reports were erroneous. Erroneous data from the reports was incorporated in the released IFU 81110294 EVOS Large…
FDA · DeviceSmith & Nephew, Inc.US Nationwide distribution in the states of CO, FL, GA, MA, MN, MO, NC, NJ,…Official notice →- 2021-11-24
US
Smith & Nephew, Inc. recalls Smith and Nephew EVOS Self-Tapping Locking Screw SST: (1)REF 72413575, 3.5MM x 75MM, and (2) REF 72413570, 3.5MM X 70MM. Sterile.
The labels on the packages of screws were switched.
FDA · DeviceSmith & Nephew, Inc.Distribution was made to AL, AZ, CA, CO, CT, FL, GA, IL, IN, KY, LA, MA, ME,…Official notice →
Other drugs & medical recalls in the United States
- 2021-10-27
US
Smiths Medical ASD Inc. recalls CADD Administration Sets, Model #21-7346-24
Product may have been manufactured with an air filter assembled in an incorrect orientation.
US
Medical Action Industries, Inc. 306 recalls Kit: Central Line Dres Change 20/Cs
The ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date.
FDA · DeviceMedical Action Industries, Inc. 306Distribution to a single US distributor in MichiganOfficial notice →US
ADRIA SRL recalls Herniatome, 17G x 15cm, Lumbar Type, Model Number 5091745
The recalling firm was notified by the contract sterilizer that the process parameters of the sterilization cycles were not followed.
FDA · DeviceADRIA SRLThe products were distributed to the following US states: NJ and NY.Official notice →US
Canon Medical System, USA, INC. recalls Canon PET-CT SCANNER, Cartesion Prime, MODEL PCD-1000A
A software problem has been identified which could result in the diagnostic imaging system not proceeding to the next actual scan even though automatic start of the next scan is specified. This could result in the…
FDA · DeviceCanon Medical System, USA, INC.US Nationwide distribution in the states of NV, AR MN.Official notice →US
GE Healthcare, LLC recalls SIGNA Pioneer nuclear magnetic resonance imaging system
Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.
FDA · DeviceGE Healthcare, LLCDistribution in United States to AZ, CA, FL, GA, IL, LA, MA, MD, MN, NC, NH,…Official notice →US
Stradis Medical, LLC dba Stradis Healthcare recalls Foundation Kit
Firm unable to confirm that the tenaculum devices were produced in accordance with required design and manufacturing standards.
FDA · DeviceStradis Medical, LLC dba Stradis HealthcareDistributed nationwide to VA, SC, CA, PA, MA, FL, TN, NJ, GA, AZ, IL, OH, OK,…Official notice →