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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

Par Pharmaceutical Treprostinil Injection - recalled due to Silicone Particulate Matter, USA

2 years ago •source fda.gov • details

Endo International plc announced today that one of its operating companies, Par Pharmaceutical, Inc. (Par), is voluntarily recalling one lot of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product is being recalled due to the potential for the presence of silicone particulates in the product… See more

#recall #drugs #unitedstates

Recalls Par Pharmaceutical Treprostinil Injection - recalled due to Silicone Particulate Matter Endo Interna... photo #1
312   Comments Comment

Recall notice

Megadyne Electrodes - Alert to Use for ages 12+ only, USA

2 years ago •source fda.gov • details

Megadyne issued a Class 1 Medical Device Correction to hospitals to limit the use of MEGA SOFT Universal and Universal Plus Reusable Patient Return Electrodes to patients aged 12 years or older after receiving reports of adult and pediatric patient burns following surgical procedures in which MEGA… See more

#recall #medicaldevices #unitedstates

Recalls Megadyne Electrodes - Alert to Use for ages 12+ only Megadyne issued a Class 1 Medical Device Correc... photo #1
312   Comments Comment

Recall notice

Avanos Medical MIC* Gastric-Jejunal Feeding Tube Kits recalled due to potential lack of sterility, USA

2 years ago •source fda.gov • details

Avanos Medical, Inc. voluntarily recalled specific lots of MIC* Gastric – Jejunal Feeding Tube Kits on Jan. 16, 2024. These kits include Nurse Assist supplied syringes, pre-filled with sterile water, essential for inflating the retention balloon of the feeding tube. This recall initiated in direct response to… See more

#recall #medicaldevices #unitedstates

Recalls Avanos Medical MIC* Gastric-Jejunal Feeding Tube Kits recalled due to potential lack of sterility Av... photo #1
312   Comments Comment

Recall notice

Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to lack of sterility assurance, USA

2 years ago •source fda.gov • details

Brassica Pharma Pvt. Ltd. is voluntarily recalling the Eye Ointment products listed below with expiration dates ranging from February 2024 to September 2025. The products are being recalled due to a lack of sterility assurance. These products were distributed nationwide to wholesalers, retailers, and via the product… See more

#cvspharmacy #recall #walmart #drugs #unitedstates

Recalls Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to lack of sterility assurance Brassi... photo #1
312   Comments Comment

Recall notice

Alipotec King Alipotec Raiz de Tejocote - recalled due to Yellow oleander, USA

2 years ago •source fda.gov • details

Backstage Center is issuing a recall of approximately 280 Bottles of Alipotec Raiz de Tejocote, dietary supplements, that are labeled with the "Alipotec King" sticker. This recall is being initiated because FDA analysis found that the product contains toxic yellow oleander. The product has been exclusively distributed… See more

#vitamins #amazon #recall #unitedstates

Recalls Alipotec King Alipotec Raiz de Tejocote - recalled due toYellow oleander Backstage Center is issuing... photo #1
312   Comments Comment

Recall notice

H&Natural Brand Products - recalled due to Yellow oleander, USA

2 years ago •source fda.gov • details

San Luis, AZ, G.A. Mart dba H&Natural, is voluntarily recalling 2 lots of H&NATURAL TejoRoot, 10g pills, and 2 lots of H&NATURAL Brazil Seed, .167g Seeds to the consumer level. The products have been found via random FDA testing to contain yellow oleander, a poisonous plant native… See more

#vitamins #amazon #walmart #recall #unitedstates

Recalls H&Natural Brand Products - recalled due to Yellow oleander San Luis, AZ, G.A. Mart dba H&Natural, is... photo #1
312   Comments Comment

Recall notice

Nordic Naturals Baby's Vitamin D3 - recalled due to Elevated level of Vitamin D3 dosage, USA

2 years ago •source fda.gov • details

Nordic Naturals is voluntarily recalling one lot of Nordic Naturals Baby's Vitamin D3 Liquid. This recall is being conducted due to a manufacturing error that resulted in an elevated level of Vitamin D3 dosage or super potent dose. There have been no reports of adverse events to… See more

#vitamins #recall #unitedstates

Recalls Nordic Naturals Baby’s Vitamin D3 - recalled due to Elevated level of Vitamin D3 dosage Nordic Natur... photo #1
312   Comments Comment

Recall notice

Sustain and Schwinnng male enhancement capsules - recalled due to undeclared Tadalafil and Nortadalafil, USA

2 years ago •source fda.gov • details

"Today The World" is voluntarily recalling two lots of Sustain herbal dietary supplement capsules and one lot of Schwinnng capsules to the consumer level. FDA analysis has found the products to contain undeclared Tadalafil and Nortadalafil. Products were distributed online nationwide in the USA. To date, no… See more

#recall #drugs #unitedstates

Recalls Sustain and Schwinnng male enhancement capsules - recalled due to undeclared Tadalafil and Nortadala... photo #1
312   Comments Comment

Recall notice

Arize male enhancement capsules - recalled due to undeclared Nortadalafil, USA

2 years ago •source fda.gov • details

"Today The World" is voluntarily recalling one lot of Arize Herbal Dietary Supplement capsules to the consumer level. FDA analysis has found the products to contain undeclared Nortadalafil. The product was distributed online via their website in the USA. To date, no adverse events have been reported.… See more

#recall #drugs #unitedstates

Recalls Arize male enhancement capsules - recalled due to undeclared Nortadalafil "Today The World” is volun... photo #1
312   Comments Comment

Recall notice

Covidien and Cardinal Health Urology and room kits and trays Update - recalled due to potential lack of sterility assurance, USA

2 years ago •source fda.gov • details

Nurse Assist, LLC voluntary product recall (which included products supplied to Cardinal Health used in Covidien and Cardinal Health™ brand kits and trays), Cardinal Health issued a medical device recall on December 5, 2023, for its Covidien and Cardinal Health™ brand urology and operating room-specific kits and… See more

#recall #medicaldevices #unitedstates

Recalls Covidien and Cardinal Health Urology and room kits and trays Update - recalled due to potential lack... photo #1
312   Comments Comment

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