Resource Optimization & Innovation LLC recalls Regard IV Start Kit for preparing and/or dressing a peripheral vein intravenous access site
A kit component, the PDI Prevantics Swab, was recalled.
Read the official notice →- Date
- 2022-04-27
- Country
- United States
- Brand
- Resource Optimization & Innovation LLC
- Product
- Regard IV Start Kit for preparing and/or dressing a peripheral vein intravenous access site
- Classification
- Class II
- Units
- US distribution to two consignees located in Missouri
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2022-04-27
USMicrobiologics Inc recalls Inactivated macrolide-resistant Mycoplasma genitalium
The QC process was not adequate for the specification range.
FDA · DeviceMicrobiologics IncUS Nationwide distribution in the states of NV and VT.Official notice →- US
Microbiologics Inc recalls Inactivated macrolide and quinolone-resistant Mycoplasma genitalium
QC process was not adequate for the specification range.
- US
Qiagen Sciences LLC recalls therascreen KRAS RGQ PCR Kit (24) Model Number(s): REF 870021 (US IVD)
False positive or false negative G12C (12CYS) mutation result for the KRAS Mutation Status resulting from Flags/Warnings may invalidate the result for one or more individual mutation target of the kit.
- US
Terumo Cardiovascular Systems Corp recalls Cardiovascular Procedure Kit catalog # 76645 & 73806
Potential for Cardiovascular Procedure Kit packaging damage that occurred during shipping.
FDA · DeviceTerumo Cardiovascular Systems CorpUS Nationwide distribution in the states of CA and IN.Official notice → - US
Baxter Healthcare Corporation recalls Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.
Product is mislabeled as self-righting Luer slip tip caps, yellow.
FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide distribution in the states of FL, GA,…Official notice → - US
Matrix Medical Network recalls Matrix Clinical Solution At-Home COVID-19 Test
Due to COVID-19 Test not being authorized for home sample collection.
FDA · DeviceMatrix Medical NetworkU.S.: AL, AZ, CA, CO, CT, DC, DE, FL, GA, LA, MA, MD, MI, MN, NH, NJ, NY, OH,…Official notice →