TriMed Inc. recalls TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref:…
Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
Read the official notice →- Date
- 2024-05-22
- Country
- United States
- Brand
- TriMed
- Product
- TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref:…
- Classification
- Class II
- Units
- US Nationwide distribution in the states of AK, AR, AZ, CA, FL, HI, IL, LA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 TriMed recalls
- 2024-02-07
USTriMed Inc. recalls Volar Bearing Plate. REF: VBEAL-3-7N, VBEAL-5-7N, VBEAL-3-7S, VBEAL-5-7S, VBEAL-7-7S, VBEAL-3-7W, VBEAL-5-7W, VBEAR-3-7N, VBEAR-5-7-N,…
Plates, part of a wrist fixation system, are affixed during surgery with bearings that may pop out from distal peg holes.
- 2023-02-15
- US
TriMed Inc. recalls RipCord Syndesmosis Button, REF: STA001K
Overly aggressive tension on the pull suture, while passing the medial button through a bone/soft tissue tunnel across the fibula and tibia, can exceed its strength causing it to break.
FDA · DeviceTriMed Inc.US Nationwide distribution in the states of IL, PA, TX, GA, TN, AL, MO, FL,…Official notice →
Other drugs & medical recalls in the United States
- 2024-05-22
- US
Wishbone Medical, Inc. recalls WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.
The products in this lot are incorrectly packed with a Stainless-Steel implant instead of a Titanium implant as the packaging and part number indicated.
FDA · DeviceWishbone Medical, Inc.US distribution to Florida, New Jersey and Connecticut.Official notice → - US
MEDLINE INDUSTRIES, LP - Northfield recalls Namic FLUID DELIVERY SET, REF 91300040
Products have a lack of sterility assurance.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of AL, FL, KY, MS, TX, WA, WI, NC,…Official notice → - US
- US
Ossur H / F recalls RKN130002, RHEO KNEE 2 YR WARRANTY, MD, CE, External lower limb prosthetic component
Due to firmware issues with the prosthetic knee, there is the potential for unintended warnings and device shutdown which could result in patient falls.
FDA · DeviceOssur H / FUS Nationwide distribution in the states of AL, AZ, CA, CO, DE, FL, GA, HI,…Official notice → - US
Boston Scientific Corporation recalls Expo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (5PKX3), REF H749085263002; cardiac catheter
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane layer delaminating and in some instances material…
FDA · DeviceBoston Scientific CorporationWorldwide distribution. US, US Territories, EMEA, Canada, LATAM and Asia…Official notice → - US
Pharma Nobis LLC recalls Meijer Magnesium Citrate Saline Laxative Oral Solution Dye Free, Sugar Free Grape, 10 fl. oz bottle, Distributed by: Meijer Distribution…
Microbial Contamination of Non-Sterile Products - Presence of Acetobacter nitrogenifigens bacteria