Emergency Products & Research recalls O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.
Failure of adhesive to secure the pole insert.
Read the official notice →- Date
- 2024-04-03
- Country
- United States
- Brand
- Emergency Products & Research
- Product
- O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.
- Classification
- Class II
- Units
- US Nationwide distribution in the states of CA, CO, FL, GA, IL, IN, KS, MA,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
Other drugs & medical recalls in the United States
- 2024-04-10
US
B. Braun Medical Inc recalls Lactated Ringer's Injection USP, 1000mL, EXCEL CONTAINER, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7750-00
Lack of assurance of sterility: bags have the potential to leak..
US
Glenmark Pharmaceuticals Inc., USA recalls Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 Capsules per bottle, Rx Only,…
Failed Dissolution Specifications: Out of Specification (OOS) was reported in test of dissolution at the 12th month time point in long term stability study.
- 2024-04-03
US
Boston Scientific Corporation recalls OptiCross Coronary Imaging Catheter, REF H749518080120
Certain batches of Opticross 40MHz Coronary Imaging Catheters manufactured using an incorrect voltage setting, which may have resulted in decreased image brightness.
FDA · DeviceBoston Scientific CorporationInternational distribution to the country of Japan.Official notice →US
Medical Action Industries, Inc. 306 recalls IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.
The kits contain saline flush syringes which were recalled by the supplier.
FDA · DeviceMedical Action Industries, Inc. 306US Nationwide distribution in the states of MN and ND. There as no…Official notice →US
Puritan Medical Products Company, Llc recalls HydroFlock Sterile Flocked Collection Device, Part Number 25-3317-H.
It was discovered through a customer complaint that mislabeled product was distributed. Puritan distributed product labelled as 25-3317-H lot S1014 which contained product code 25-3317-U in all packages.
FDA · DevicePuritan Medical Products Company, LlcWorldwide - US Nationwide distribution in the states of AL, CA, FL, GA, IA,…Official notice →US
Boston Scientific Corporation recalls Boston Scientific iSLEEVE EXPANDABLE Introducer Set REF H74939349140, facilitates femoral access to the vascular system
Boston Scientific is conducting a removal of specific batches of the iSLEEVETM 14F Expandable Introducer Set due to complaints associated with a hemostatic valve leak.
FDA · DeviceBoston Scientific CorporationWorldwide distribution - US Nationwide and the countries of Canada.Official notice →