Recalls

458 topics in this forum

1. Heart Pump Correction: Abiomed Issues Correction for Automated Impella Controllers

   By FDA Recalls, June 11
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   • FDA Recalls
   • June 11

3. Early Alert: Positive Pressure Breathing Device Issue from Baxter

   By FDA Recalls, June 11
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   • 50 views
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   • FDA Recalls
   • June 11

4. FDA Approves Labeling Changes for Over-the-Counter (OTC) Weight Loss Drug alli (Orlistat) to Warn of Risk of Kidney Stones and Kidney Injury

   By FDA Recalls, June 10
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   • 48 views
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   • FDA Recalls
   • June 10

5. BD Issues Nationwide Recall for Specific Lots of ChloraPrep™ Clear Single Sterile 1 mL and FREPP™ Clear 1.5 mL Applicators Due to Microbial Contamination

   By FDA Recalls, June 8
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   • 43 views
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   • FDA Recalls
   • June 8

6. Early Alert: Breathing Circuit Set Issue from Hamilton Medical

   By FDA Recalls, June 8
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   • 47 views
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   • FDA Recalls
   • June 8

7. Anesthesia Delivery Systems Recall: GE HealthCare Issues Correction for Certain Carestations due to Risk of Ineffective Ventilation When Used in Volume Control Ventilation (VCV) Mode 

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

8. Early Alert: Infant Resuscitation System Issue from GE HealthCare

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

9. Haleon Issues Voluntary Nationwide Recall of Gas-X Extra Strength Softgels 125mg, 120 ct. and 72 ct.

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

10. Anesthesia Kit Correction: Becton Dickinson Issues Correction for BD Spinal Trays Containing Bupivacaine Ampules

    By FDA Recalls, June 3
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    • 52 views
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    • FDA Recalls
    • June 3

11. UPDATE: Hintermann Series H3 Total Ankle Replacement Has a Higher-Than-Expected Risk of Device Failure: FDA Safety Communication

    By FDA Recalls, June 3
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    • 53 views
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    • FDA Recalls
    • June 3

12. Early Alert: Catheter Introducer Kit Issue from Abiomed

    By FDA Recalls, June 2
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    • 51 views
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    • FDA Recalls
    • June 2

13. Pediatric Care Bed Correction: KayserBetten Issues Correction for KayserBett IDA Beds

    By FDA Recalls, May 29
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    • 70 views
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    • FDA Recalls
    • May 29

14. Dexcom Uncovers Theft of Scrapped Product, Notifies Potentially Impacted Users

    By FDA Recalls, May 29
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    • 50 views
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    • FDA Recalls
    • May 29

15. Early Alert: Heart Pump Issue from Abiomed

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

16. Early Alert: IV Tubing Set Issue from ICU Medical

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

17. Manifold Recall: Medline Removes Namic Star Off Handle Manifolds 

    By FDA Recalls, May 26
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    • 46 views
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    • FDA Recalls
    • May 26

18. Dialysis Catheter Kit Recall: Arrow International Removes Dialysis Catheter Kits Containing Merit Medical Splittable Sheath Introducers

    By FDA Recalls, May 26
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    • 57 views
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    • FDA Recalls
    • May 26

19. Insulet Initiates Voluntary Medical Device Correction for Certain Omnipod® Pods in the U.S. and Affected International Markets

    By FDA Recalls, May 26
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    • 54 views
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    • FDA Recalls
    • May 26

20. стоимость грузоперевозок

    By stoimost_kdma, May 25
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    • 49 views
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    • stoimost_kdma
    • May 25

21. Ventilator Recall: React Health Removes VOCSN V+Pro Ventilators

    By FDA Recalls, May 21
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    • 51 views
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    • FDA Recalls
    • May 21

22. Automated Compounding System Recall: Omnicell Removes Syringe Labels Used with the i.v.STATION Automated Compounding System

    By FDA Recalls, May 21
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    • 54 views
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    • FDA Recalls
    • May 21

23. Early Alert: Heart Pump Controller Issue from Abiomed

    By FDA Recalls, May 21
    • 0 replies
    • 50 views
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    • FDA Recalls
    • May 21

24. Thoracic Stent Graft Recall: Bolton Medical Removes Relay Pro System

    By FDA Recalls, May 20
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    • 49 views
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    • FDA Recalls
    • May 20

25. Early Alert: Anesthesia Machine Issue from Draeger, Inc.

    By FDA Recalls, May 15
    • 0 replies
    • 90 views
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    • FDA Recalls
    • May 15

26. Sun Pharmaceutical Industries, Inc. (Sun Pharma) Initiates Voluntary U.S. Nationwide Recall of DOXOrubicin Hydrochloride Liposome Injection 50mg/25 mL Due To Potential Presence of Glass Particles

    By FDA Recalls, May 13
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    • 48 views
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    • FDA Recalls
    • May 13