Stradis Medical, LLC dba Stradis Healthcare recalls NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5"; Part Number: ZZ-0700
The sterile barrier may be compromised.
Read the official notice →- Date
- 2022-08-24
- Country
- United States
- Brand
- Stradis Medical, LLC dba Stradis Healthcare
- Product
- NARMD MEDICAL DEPOT Forceps - Kelly Straight 5.5"; Part Number: ZZ-0700
- Classification
- Class II
- Units
- US Nationwide distribution in the state of SC.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Stradis Medical, LLC dba Stradis Healthcare recalls
- 2022-12-21
USStradis Medical, LLC dba Stradis Healthcare recalls HENRY SCHEIN, Vas Reversal Pack, Item No.888-2549,
Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.
FDA · DeviceStradis Medical, LLC dba Stradis HealthcareUS nationwide distribution, and Canada.Official notice →- 2022-04-13
- US
Stradis Medical, LLC dba Stradis Healthcare recalls Coryell Memorial Hosp Total, Joint Pack - Surgical Kit
The outer bag may be perforated or torn, which may result in a breach in the sterility of the kit.
FDA · DeviceStradis Medical, LLC dba Stradis HealthcareUS Nationwide distribution in the states of IN, TX, and PA.Official notice → - 2021-12-29
- US
Stradis Medical, LLC dba Stradis Healthcare recalls Custom Assemblies, Inc., Single Spike Tumescent Set w/o Chamber, Reorder Number CMS-1212NS Bulk
This recall has been initiated to address bulk packed, non-sterile Intravascular Administration Sets that were erroneously distributed to fill orders for the sterile version of the same Intravascular Administration Set.
FDA · DeviceStradis Medical, LLC dba Stradis HealthcareNJ, MI, MA, NY, TX, CO, NC, CT, OR, OHOfficial notice → - 2021-10-27
- 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 →
Other drugs & medical recalls in the United States
- 2022-08-24
- US
Siemens Medical Solutions USA, Inc recalls AXIOM Sensis or Sensis Vibe Combo systems as follows: System Material # AXIOM Sensis, Combo 64 6623974; AXIOM Sensis, Hemo…
The Sensis Signal Input Box provides hooks as a milled item on the bottom of the box support the possibility of mounting the Signal Input Box on an accessory rail (e.g., at the patient table), In the event the mounting…
FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide Distribution Foreign: Albania Algeria Angola Argentina Armenia…Official notice → - US
Micro Therapeutics, Inc. recalls Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only
Outer carton packaging of microcatheters were exposed to wet substance during transport.
- US
Becton Dickinson & Company recalls BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanically prohibits the…
Incorrect expiration date listed on the product labels. The expiration date listed on the product label is beyond the expiration date of the product.
FDA · DeviceBecton Dickinson & CompanyUS Nationwide Distribution CA FL GA IL MD MI OR PA PR TN TXOfficial notice → - US
Trinity Sterile, Inc. recalls Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708
Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy
FDA · DeviceTrinity Sterile, Inc.US Nationwide distribution in the states of FL, PA.Official notice → - US
Family Dollar Stores, Llc. recalls KY JELLY LUBRICANT 2 FL OZ, SKU 901443
Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
FDA · DeviceFamily Dollar Stores, Llc.Product distributed to Family Dollar retail stores in US nationwide.Official notice → - US
Luminex Corporation recalls ARIES SARS-CoV-2 Assay
SARS-CoV-2 assay that detects SARS-CoV-2 ORF1ab and N genes may not detect the ORF1ab gene. A positive results if either SARS-CoV-2 genes is detected, but If both genes are mistakenly not detected, a false negative…
FDA · DeviceLuminex CorporationU.S. Nationwide distribution in the states of NE, TX, MS, TN, KY, ME, CA.Official notice →