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Safety Reports: Recall

Updated:

Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to Due to Potential Lack of Sterility Assurance., USA

8 months ago •source fda.gov • details

Recall notice

Company name: Brassica Pharma Pvt. Ltd.
Brand name: Multiple brands
Product recalled: Eye ointment products
Reason of the recall: Due to Potential Lack of Sterility Assurance.
FDA Recall date: February 26, 2024
Recall details: Company Announcement FOR IMMEDIATE RELEASE – 12 February, 2024 – Thane, Maharashtra, India,… See more

#recall #drugs #unitedstates

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

10 months ago •source fda.gov • details

Recall notice

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

Hospira Sodium bicarbonate & Atropine sulfate injections - recalled due to the presence of glass particulate matter photo #1

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

10 months ago •source fda.gov • details

Recall notice

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

#recall #drugs #unitedstates

Americaine Benzocaine Topical Anesthetic Spray - recalled due to Presence of benzene photo #1

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

10 months ago •source fda.gov • details

Recall notice

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

Bleomycin for Injection, USP 15 Units Single Dose ONCO-TAIN™ Glass Fliptop Vial - recalled due to Presence of Glass Particulate Matter photo #1

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

10 months ago •source fda.gov • details

Recall notice

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

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

Blue Ridge Beef Kitten Grind, Kitten Mix, and Puppy Mix - recalled due Salmonella and Listeria monocytogenes photo #1

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

10 months ago •source fda.gov • details

Recall notice

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

ResMed Masks with magnets - recalled due to magnetic interference near certain implants and medical devices photo #1

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

10 months ago •source fda.gov • details

Recall notice

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

Medline, LP Tracheostomy Care and Cleaning Trays - recalled due to Device & Drug Safety photo #1

Busse Hospital Disposals Medical Device Kits and Trays - recalled due to device & drug safety, USA

10 months ago •source fda.gov • details

Recall notice

On November 21, 2023, Busse Hospital Disposals initiated a nationwide recall of medical device kits and trays containing (1) Nurse Assist part 6240, Stericare 100ML Sterile Saline Botle. This is the only saline contained in the trays/kits. Busse initiated this recall in direct response to Nurse Assist… See more

#recall #medicaldevices #unitedstates

Busse Hospital Disposals Medical Device Kits and Trays - recalled due to device & drug safety photo #1

Citi Trade Int’l Limited Notoginseng Formula Special Gout Granule - recalled due to undeclared drugs, USA

10 months ago •source fda.gov • details

Recall notice

8th Avenue Pharmacy is voluntarily recalling all lots within the expiry of Notoginseng Formula Special Gout Granule, distributed by 8th Avenue Pharmacy, to the consumer level. The products have been found to contain undeclared diclofenac and dexamethasone from FDA laboratory analysis. Notoginseng Formula Special Gout Granule was… See more

#recall #amazon #unitedstates

Citi Trade Int’l Limited Notoginseng Formula Special Gout Granule - recalled due to undeclared drugs photo #1

TYSON Tonic Kava & Kratom Blend shots - recalled due to unapproved food additive: kratom, USA

11 months ago •source accessdata.fda.gov • details

Recall notice

FDA announced the recall of 15,000 units of TYSON Tonic Kava & Kratom Blend shots by LGNDS LLC because the products contain kratom (an unapproved food additive) and pH is over 5.0. The process authority letter classified product as acidified and pH cannot exceed 3.30. These products… See more

#supplement #recall #unitedstates

TYSON Tonic Kava & Kratom Blend shots - recalled due to unapproved food additive: kratom photo #1

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