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endoscope-instrument-recall:-olympus-removes-single-use-guide-sheath-kits-due-to-risk-for-radiopaque-guide-sheath-tip-detaching-during-procedures FDA
  • February 28, 2025

Endoscope Instrument Recall: Olympus Removes Single Use Guide Sheath Kits Due to Risk for Radiopaque Guide Sheath Tip Detaching During Procedures

Olympus Guide Sheath Kits collect samples from breathing organs through an endoscope. The tip of the guide sheath may detach…
regard-newborn-kit-recall:-roi-cps,-llc-removes-certain-newborn-kits-due-to-a-recalled-component,-the-neo-tee-t-piece-resuscitator-with-an-undersized-controller-spring FDA
  • February 28, 2025

Regard Newborn Kit Recall: ROi CPS, LLC Removes Certain Newborn Kits Due to a Recalled Component, the Neo-Tee T-Piece Resuscitator With An Undersized Controller Spring

ROi newborn kits include Neo-Tee T-Piece Resuscitators. The Neo-Tee may have an undersized controller spring that could affect patient breathing…
natural-dior-llc-issues-voluntary-nationwide-recall-of-vitafer-l-gold-liquid-due-to-presence-of-undeclared-tadalafil FDA
  • February 26, 2025

Natural Dior LLC Issues Voluntary Nationwide Recall of Vitafer-L Gold Liquid Due to Presence of Undeclared Tadalafil

February 25, 2025 – Natural Dior LLC, is voluntarily recalling the affected lots of Vitafer-L Gold Liquid, a dietary supplement…
central-admixture-pharmacy-services-(caps)-issues-nationwide-recall-of-phenylephrine-40-mg-added-to-0.9%-sodium-chloride-250-ml-in-250-ml-excel-bags-due-to-visible-black-particulate-matter-in-a-single-sealed-vial FDA
  • February 25, 2025

Central Admixture Pharmacy Services (CAPS) Issues Nationwide Recall of Phenylephrine 40 mg Added to 0.9% Sodium Chloride 250 mL in 250 mL Excel Bags Due to Visible Black Particulate Matter in a Single-Sealed Vial

February 24, 2025 – Bethlehem, PA. Central Admixture Pharmacy is recalling three lots of Phenylephrine 40 mg added to 0.9%…
lyons-magnus-recalls-lyons-readycare-and-sysco-imperial-frozen-supplemental-shakes-manufactured-by-third-party-because-of-possible-health-risk FDA
  • February 22, 2025

Lyons Magnus Recalls Lyons ReadyCare and Sysco Imperial Frozen Supplemental Shakes Manufactured by Third Party Because of Possible Health Risk

Lyons Magnus LLC (“Lyons Magnus”) today announced that it is voluntarily recalling 4 oz. Lyons ReadyCare and Sysco Imperial Frozen…
kayco-issues-an-allergy-alert-on-undeclared-milk-in-limited-units-of-glicks-dark-chocolate-conettos FDA
  • February 21, 2025

Kayco Issues an Allergy Alert on Undeclared Milk in Limited Units of Glicks Dark Chocolate Conettos

Kayco, a Bayonne NJ company is recalling their Glicks Dark Chocolate Conettos because it may contain undeclared milk. People who…
pacemaker-recall:-boston-scientific-corporation-recalls-accolade-pacemaker-devices-due-to-a-manufacturing-issue-that-may-lead-to-early-device-replacement FDA
  • February 21, 2025

Pacemaker Recall: Boston Scientific Corporation Recalls Accolade Pacemaker Devices Due to a Manufacturing Issue That May Lead to Early Device Replacement

Boston Scientific is recalling pacemakers due to a manufacturing issue that may cause early device replacement.
accolade-pacemaker-devices-by-boston-scientific-and-potential-need-for-early-device-replacement-–-fda-safety-communication FDA
  • February 21, 2025

Accolade Pacemaker Devices by Boston Scientific and Potential Need for Early Device Replacement – FDA Safety Communication

Read the FDA’s recommendations related to Accolade pacemaker devices by Boston Scientific and a potential need for early device replacement.
kedake-inc-issues-allergy-alert-on-undeclared-sesame,-soy,-wheat,-yellow-no-5,-yellow-no-6,-and-red-no.-6-in-botana-mix-snacks FDA
  • February 20, 2025

Kedake Inc. Issues Allergy Alert on Undeclared Sesame, Soy, Wheat, Yellow No. 5, Yellow No. 6, and Red No. 6 in Botana Mix Snacks

KEDAKE, INC. of Houston, TX is recalling it’s 2 lb packages of Las Ollas Botana Mix Snacks because they may…
one-source-nutrition,-inc.-issues-voluntary-nationwide-recall-of-vitality-capsules-due-to-presence-of-undeclared-sildenafil-and-tadalafil FDA
  • February 20, 2025

One Source Nutrition, Inc. Issues Voluntary Nationwide Recall of Vitality Capsules Due to Presence of Undeclared Sildenafil and Tadalafil

Benton, Arkansas – 02/2019/2025 –One Source Nutrition is voluntarily recalling all lots of Vitality capsules to the Consumer level. FDA…