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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

Leiters Health Vancomycin, Phenylephrine & Fentanyl IV Bags - recalled due to potential double drug potency, USA

2 years ago •source fda.gov • details

Leiters Health is voluntarily recalling 33 lots of products to the user level. The recalled batches of vancomycin IV bags, phenylephrine IV bags, and fentanyl IV bags are being recalled due to the potential for superpotency because they may contain twice the labeled amount of drug. The… See more

#recall #drugs #unitedstates

Recalls Leiters Health Vancomycin, Phenylephrine & Fentanyl IV Bags - recalled due to potential double drug... photo #1
313   Comments Comment

Recall notice

3-D Pet Products Parrot Food - recalled due to potential Salmonella contamination, Lincoln, Kansas, USA

2 years ago •source fda.gov • details

Greeley, CO – D&D Commodities Ltd. is voluntarily recalling one lot of 3-D® Pet Products Premium Parrot Food, due to potential Salmonella contamination. The affected parrot food product is packaged in clear plastic jars and was distributed to retailers and distributors in the following states: Arizona, Arkansas,… See more

#recall #petfood #lincoln #kansas #unitedstates

Recalls 3-D Pet Products Parrot Food - recalled due to potential Salmonella contamination Greeley, CO – D&D... photo #1
1   Comments Comment

Recall notice

Atrium Express Drains - recalled due to unverified sterility of provided syringes, USA

2 years ago •source fda.gov • details

Getinge / Atrium Medical Corporation notified affected customers of a nationwide recall (medical device correction) for certain Atrium Express Dry Suction Dry Seal Chest Drains in response to a voluntary medical device recall initiated by a supplier, Nurse Assist. On November 8, 2023, Getinge received notice from… See more

#recall #medicaldevices #unitedstates

Recalls Atrium Express Drains - recalled due to unverified sterility of provided syringes Getinge / Atrium M... photo #1
312   Comments Comment

Recall notice

Blue Ridge Beef Kitten Grind, Kitten Mix, and Puppy Mix Update - recalled due to Salmonella and Listeria, USA

2 years ago •source fda.gov • details

Blue Ridge Beef is expanding their recall to include additional lot numbers due to contamination of Salmonella and Listeria monocytogenes. The products were distributed between 11/14/2023 – 12/20/2023. These products were packaged in clear plastic and sold primarily in retail stores located in the states of: CT,… See more

#recall #animalveterinary #paintlick #kentucky #unitedstates

Recalls Blue Ridge Beef Kitten Grind, Kitten Mix, and Puppy Mix Update - recalled due to Salmonella and List... photo #1
  Comments Comment

Recall notice

Hospira Sodium bicarbonate & Atropine sulfate injections - recalled due to the presence of glass particulate matter, USA

2 years ago •source fda.gov • details

Hospira, Inc., a Pfizer company, is voluntarily recalling the lots listed in the table below of 4.2% Sodium Bicarbonate Injection, USP ABBOJECT® Glass Syringe, 5 mEq/10 mL; 8.4% Sodium Bicarbonate Injection, USP Lifeshield® ABBOJECT® Glass Syringe, 50 mEq/50 mL; and Atropine Sulfate Injection, USP Lifeshield® ABBOJECT® Glass… See more

#recall #drugs #unitedstates

Recalls Hospira Sodium bicarbonate & Atropine sulfate injections - recalled due to the presence of glass par... photo #1
312   Comments Comment

Recall notice

Americaine Benzocaine Topical Anesthetic Spray - recalled due to Presence of benzene, USA

2 years ago •source fda.gov • details

Insight Pharmaceuticals, a Prestige Consumer Healthcare Inc. company ("Insight"), is voluntarily recalling one lot of Americaine® 20% Benzocaine Topical Anesthetic Spray to the consumer level. While benzene is not an ingredient in any Americaine® 20% Benzocaine Topical Anesthetic Spray products, a recent review by our manufacturer and… See more

#drugs #recall #unitedstates

Recalls Americaine Benzocaine Topical Anesthetic Spray - recalled due to Presence of benzene Insight Pharmac... photo #1
312   Comments Comment

Recall notice

Bleomycin for Injection, USP 15 Units Single Dose ONCO-TAIN™ Glass Fliptop Vial - recalled due to Presence of Glass Particulate Matter, USA

2 years ago •source fda.gov • details

Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of Bleomycin for Injection, USP 15 units Single Dose ONCO-TAIN™ Glass Fliptop Vial, to the user level. The recall was initiated due to a confirmed customer report for the presence of glass particulate within a single vial.… See more

#recall #drugs #unitedstates

Recalls Bleomycin for Injection, USP 15 Units Single Dose ONCO-TAIN™ Glass Fliptop Vial - recalled due to Pr... photo #1
312   Comments Comment

Recall notice

Blue Ridge Beef Kitten Grind, Kitten Mix, and Puppy Mix - recalled due Salmonella and Listeria monocytogenes, Whaleyville, Maryland 21872, USA

2 years ago •source fda.gov • details

Blue Ridge Beef is recalling all lot numbers and used by dates between N24 1124 to N24 1224 due to contamination of Salmonella and Listeria monocytogenes. The products were distributed between 11/14/2023 – 12/20/2023. These products were packaged in clear plastic and sold primarily in retail stores… See more

#dogfood #catfood #recall #petfood #whaleyville #maryland #unitedstates

Recalls Blue Ridge Beef Kitten Grind, Kitten Mix, and Puppy Mix - recalled due Salmonella and Listeria monoc... photo #1
  Comments Comment

Recall notice

ResMed Masks with magnets - recalled due to magnetic interference near certain implants and medical devices, USA

2 years ago •source fda.gov • details

ResMed (NYSE: RMD, ASX: RMD) is conducting a voluntary global field action to update its guides for all masks with magnets to inform users about potential magnetic interference when magnets are near certain implants and medical devices in the body. This voluntary field correction does not require… See more

#recall #medicaldevices #unitedstates

Recalls ResMed Masks with magnets - recalled due to magnetic interference near certain implants and medical... photo #1
312   Comments Comment

Recall notice

Medline, LP Tracheostomy Care and Cleaning Trays - recalled due to Device & Drug Safety, USA

2 years ago •source fda.gov • details

Medline Industries, LP. announced a voluntary nationwide recall on October 10th, 2023, of several lots and SKUs of Tracheostomy Care and Cleaning Trays. The Tracheostomy Care and Cleaning Trays include a tracheostomy brush as a component that may have sharp edges at the tip that can puncture… See more

#recall #medicaldevices #unitedstates

Recalls Medline, LP Tracheostomy Care and Cleaning Trays - recalled due to Device & Drug Safety Medline Indu... photo #1
312   Comments Comment

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