Recalls

203 topics in this forum

1. 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
   • 0 replies
   • 13 views
   • 
   • FDA Recalls
   • June 4

3. 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
   • 0 replies
   • 36 views
   • 
   • FDA Recalls
   • May 27

4. 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
   • 0 replies
   • 25 views
   • 
   • FDA Recalls
   • May 23

5. 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
   • 0 replies
   • 28 views
   • 
   • FDA Recalls
   • May 23

6. 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
   • 0 replies
   • 17 views
   • 
   • FDA Recalls
   • May 22

7. 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
   • 0 replies
   • 34 views
   • 
   • FDA Recalls
   • May 12

8. Компания клининговая

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

9. 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
   • 0 replies
   • 32 views
   • 
   • FDA Recalls
   • May 7

10. 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
    • 35 views
    • 
    • FDA Recalls
    • May 6

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

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

12. 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
    • 30 views
    • 
    • FDA Recalls
    • April 24

13. Early Alert: Intravascular PICC Catheter Issue from BD

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

14. Early Alert: Diagnostic Intravascular Catheter Issue from Conavi

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

15. 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
    • 0 replies
    • 47 views
    • 
    • FDA Recalls
    • April 18

16. 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
    • 44 views
    • 
    • FDA Recalls
    • April 18

17. Заказать уборку квартиры

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

18. 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
    • 0 replies
    • 46 views
    • 
    • FDA Recalls
    • April 7

19. 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
    • 66 views
    • 
    • FDA Recalls
    • April 7

20. Vascular Cannula Recall: Medtronic Removes Aortic Root Cannula Due to Unexpected Loose Material in the Male Luer

    By FDA Recalls, March 31
    • 0 replies
    • 65 views
    • 
    • FDA Recalls
    • March 31

21. Safe Use of Megadyne Mega 2000 and Mega Soft Patient Return Electrodes - Letter to Health Care Providers

    By FDA Recalls, March 26
    • 0 replies
    • 59 views
    • 
    • FDA Recalls
    • March 26

22. Endotracheal Tube Recall: Smiths Medical Removes Intubation ORAL/NASAL Endotracheal Tubes Due to Smaller Than Expected Tube Diameter That May Cause Underventilation

    By FDA Recalls, March 25
    • 0 replies
    • 115 views
    • 
    • FDA Recalls
    • March 25

23. Update on Alert: Atherectomy Catheter System Issue from Bard Peripheral Vascular

    By FDA Recalls, March 20
    • 0 replies
    • 94 views
    • 
    • FDA Recalls
    • March 20

24. Infusion Pump Software Correction: Becton, Dickinson and Company (BD) Issues Correction for BD Alaris Systems Manager and Care Coordination Engine Infusion Adapter Software Due to Risk for Outdated Automated Programming Requests to Load

    By FDA Recalls, March 20
    • 0 replies
    • 47 views
    • 
    • FDA Recalls
    • March 20

25. Early Alert: Aspiration System Issue from Calyxo

    By FDA Recalls, March 20
    • 0 replies
    • 140 views
    • 
    • FDA Recalls
    • March 20

26. Update on Alert: Infusion Pump Issue from Baxter Healthcare Corporation

    By FDA Recalls, March 20
    • 0 replies
    • 64 views
    • 
    • FDA Recalls
    • March 20