Recalls

210 topics in this forum

1. Infusion Pump Correction: Baxter Updates Instructions for Use for Novum IQ Large Volume Pump due to Potential for Underinfusion

   By FDA Recalls, June 6
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   • 41 views
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   • FDA Recalls
   • June 6

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   By 888starz_gpKt, June 5
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   • 37 views
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   • 888starz_gpKt
   • June 5

4. Infusion Pump Recall: Infusion Pump Thermal Damage Issue from Smiths Medical

   By FDA Recalls, June 5
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   • 38 views
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   • FDA Recalls
   • June 5

5. Anesthesia Breathing Circuit Kit Correction: Draeger, Inc. Updates Use Instructions for VentStar Flex and Anesthesia Circuit Kits Due to Cracks in Hose That May Cause Inadequate Ventilation

   By FDA Recalls, June 5
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   • 36 views
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   • FDA Recalls
   • June 5

6. Infusion Pump Recall: False Alarm Issue with Infusion Pump from Smiths Medical

   By FDA Recalls, June 5
   • 0 replies
   • 27 views
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   • FDA Recalls
   • June 5

7. Infusion Pump Recall: Infusion Pump Intermittent Connection Issue from Smiths Medical

   By FDA Recalls, June 5
   • 0 replies
   • 33 views
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   • FDA Recalls
   • June 5

8. Flexible Tracheostomy Tube Recall: Medtronic Removes Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable Inner Cannula Due to Risk for Disconnection of the Flange from the Device Cannula

   By FDA Recalls, June 5
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   • 31 views
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   • FDA Recalls
   • June 5

9. Amneal Pharmaceutical LLC Issues a Nationwide Recall of Sulfamethoxazole / Trimethoprim Tablets, USP, 400 mg/80 mg Only, Due to Microbial Contamination

   By FDA Recalls, June 4
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   • 31 views
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   • FDA Recalls
   • June 4

10. Risk of False Positive Lead Test Results with Certain Capillary Blood Collection Tubes Used with Magellan Diagnostics LeadCare Testing Systems – FDA Safety Communication

    By FDA Recalls, May 27
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    • 51 views
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    • FDA Recalls
    • May 27

11. Cetirizine or Levocetirizine: Drug Safety Communication - FDA Warns About Risk of Severe Itching After Discontinuation of Long-Term Use of Allergy Medicines

    By FDA Recalls, May 23
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    • 41 views
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    • FDA Recalls
    • May 23

12. Esophagogastric Tube Recall: BD Issues Correction for Esophagogastric Balloon Tamponade Tubes due to Challenges Removing Plastic Plugs from Rubber Lumen

    By FDA Recalls, May 23
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    • 40 views
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    • FDA Recalls
    • May 23

13. UMARY- USA.COM Issues Voluntary Nationwide Recall of UNAVY ÁCIDO HIALURÓNICO Caplets and UMOVY ÁCIDO HIALURÓNICO Caplets Due to the Presence of Undeclared Drug Ingredients Dexamethasone, Diclofenac and Omeprazole

    By FDA Recalls, May 22
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    • 32 views
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    • FDA Recalls
    • May 22

14. FDA and CDC Recommend Pause in Use of Ixchiq (Chikungunya Vaccine, Live) in Individuals 60 Years of Age and Older While Postmarketing Safety Reports are Investigated: FDA Safety Communication

    By FDA Recalls, May 12
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    • 45 views
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    • FDA Recalls
    • May 12

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    By JimmyVar, May 9
    • 0 replies
    • 59 views
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    • JimmyVar
    • May 9

16. FDA Advises Consumers, Tattoo Artists, and Retailers to Avoid Using or Selling Certain Sacred Tattoo Ink Products Contaminated with Microorganisms

    By FDA Recalls, May 7
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    • 57 views
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    • FDA Recalls
    • May 7

17. EnShiShiXiangNiShangMaoYouXianGongSi Issues Voluntary Nationwide Recall of ENDURANCE BOOST WITH HORNY GOAT WEED Capsules Due To Presence of Undeclared Propoxyphenylsildenafil and Sildenafil

    By FDA Recalls, May 6
    • 0 replies
    • 45 views
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    • FDA Recalls
    • May 6

18. Heart Pump Accessory Removal: Abbott Removes HeartMate Mobile Power Unit due to Instances of Sudden Power Loss

    By FDA Recalls, April 24
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    • 59 views
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    • FDA Recalls
    • April 24

19. Risk of False Positive Results with Certain Capillary Blood Collection Tubes Used with Magellan Diagnostics LeadCare Testing Systems – FDA Safety Communication

    By FDA Recalls, April 24
    • 0 replies
    • 45 views
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    • FDA Recalls
    • April 24

20. Early Alert: Intravascular PICC Catheter Issue from BD

    By FDA Recalls, April 18
    • 0 replies
    • 56 views
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    • FDA Recalls
    • April 18

21. Early Alert: Diagnostic Intravascular Catheter Issue from Conavi

    By FDA Recalls, April 18
    • 0 replies
    • 63 views
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    • FDA Recalls
    • April 18

22. FDA Classifies Q’Apel Medical Inc.’s Worldwide Medical Device Recall and Discontinuation of its 072 Aspiration System (Hippo) as Class I

    By FDA Recalls, April 18
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    • 61 views
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    • FDA Recalls
    • April 18

23. Amneal Pharmaceutical LLC Issues a Nationwide Recall of Ropivacaine Hydrochloride Injection, USP 500mg/100mL, Due to the Potential Presence of Particulate Matter

    By FDA Recalls, April 18
    • 0 replies
    • 59 views
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    • FDA Recalls
    • April 18

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    By uborka_llMt, April 16
    • 0 replies
    • 60 views
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    • uborka_llMt
    • April 16

25. Bausch + Lomb Announces Voluntary Recall of enVista Aspire™, enVista Envy™ and Certain enVista® Monofocal Intraocular Lenses in the U.S.

    By FDA Recalls, April 7
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    • 63 views
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    • FDA Recalls
    • April 7

26. Max Mobility / Permobil Expands Nationwide Recall of SmartDrive Speed Control Dial Due to the Motor Being Unresponsive to the User

    By FDA Recalls, April 7
    • 0 replies
    • 88 views
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    • FDA Recalls
    • April 7