Carwild Corporation recalls FABCO ORS DENTAL ROLLS, 1-1/2" STERILE, COTTON 3/8" Diameter x 1-1/2" (9.5mm x 38.1mm), packaged 5 /Pouch, 50 Pouches/Box Reorder Number:…
Sterility with new cotton source not validated
Read the official notice →- Date
- 2022-09-21
- Country
- United States
- Brand
- Carwild
- Product
- FABCO ORS DENTAL ROLLS, 1-1/2" STERILE, COTTON 3/8" Diameter x 1-1/2" (9.5mm x 38.1mm), packaged 5 /Pouch, 50 Pouches/Box Reorder Number:…
- Classification
- Class II
- Units
- US Nationwide
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Carwild recalls
- 2025-01-08
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Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
Other drugs & medical recalls in the United States
- 2022-09-28
- US
UNICHEM PHARMACEUTICALS USA INC recalls Clonidine Hydrochloride Tablets, USP, 0.3 mg, 100-count bottle, Rx Only, Manufactured by: UNICHEM LABORATORIES LTD. Pilerne Ind.…
Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,
- 2022-09-21
- US
Alcor Scientific, Inc. recalls iSED Primary Pump Tubing Spare Part Kit- (IVD) tubing is used to move sample and wash solution from the aspiration needle, through the…
Primary Pump Tubing Spare Part is incorrect. If the tubing is installed onto an ALCOR iSED ESR Analyzer, there is a potential of a biohazard leak from the iSEDs Probe Tube
FDA · DeviceAlcor Scientific, Inc.US Nationwide Distribution - FL, MA, MD, PA, SD, WI Foreign: Croatia Honduras…Official notice → - US
FUJIFILM Healthcare Americas Corporation recalls Surpria 64: Software Version V3.11, V3.22
Error 00003050 or 00003052 may occur during scanning, the captured images will not be reconstructed and the Raw Data will not be displayed in the work list.result, may result in the need for additional scanning to…
- US
Qiagen Sciences LLC recalls QIAcube Connect MDx, Model No. 9003070
During the "Load tip racks and enzymes" step of the run set-up, the info screen indicates "minimal volume to be loaded", but the indicated volume is instead the exact volume that should be loaded. Misunderstanding the…
FDA · DeviceQiagen Sciences LLCDomestic distribution to AZ, CA, CO, DE, DC, FL, GA, IA, KS, LA, MA, MD, MN,…Official notice → - US
Mallinckrodt, LLC. recalls INOmax DSIR -(delivery system) delivers INOMAX (nitric oxide for inhalation) therapy gas into the inspiratory limb of the patient…
The INOmax DSIR Delivery System, manufactured by Mallinckrodt Pharmaceuticals, is not compatible with the upgraded version of the Leoni Plus ventilator, manufactured by Lowenstein Medical. The Leoni Plus ventilator was…
FDA · DeviceMallinckrodt, LLC.Foreign Only: Argentina Australia Austria Beligum Canada Chile Columbia Czech…Official notice → - US
Philips Medical Systems (Cleveland) Inc recalls Pinnacle3 Radiation Therapy Planning System, Model numbers 870231 and 870237.
When computing a radiation dose in the system, the exported dose information is incorrect when there is more than one beam attached to the prescription and certain options are selected on the Edit Prescription screen.
FDA · DevicePhilips Medical Systems (Cleveland) IncDistribution was made to CA, FL, GA, IA, IL, MA, MD, ME, MI, MN, NJ, NM, NV,…Official notice →