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Safety Reports: Recall

Updated:

Real Time Reports

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

#recall #drugs #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

#medicaldevices #recall #unitedstates

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

Recall notice

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

2 years ago •source fda.gov • details

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

Recalls Busse Hospital Disposals Medical Device Kits and Trays - recalled due to device & drug safety On Nov... photo #1
312   Comments Comment

Recall notice

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

2 years ago •source fda.gov • details

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

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

Recall notice

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

2 years ago •source accessdata.fda.gov • details

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

#wellnesscoffee #recall #unitedstates

Recalls TYSON Tonic Kava & Kratom Blend shots - recalled due to unapproved food additive: kratom FDA announc... photo #1
312   Comments Comment

Recall notice

Garden of Life whole Food Dietary Supplements - recalled due to undeclared soy, USA

2 years ago •source accessdata.fda.gov • details

FDA announced the recall of Garden of Life whole Food Dietary Supplements by Garden Of Life Llc due to undeclared Soy. These products were distributed in the US.

The recalled products are:
- Garden of Life, FYI ULTRA, ULTIMATE Joint & Cartilage Formula, Whole Food Dietary Supplement,… See more

#vitamins #recall #unitedstates

Recalls Garden of Life whole Food Dietary Supplements - recalle due to undeclared soy FDA announced the reca... photo #1
314   Comments Comment

Recall notice

InvaGen Pharmaceuticals Inc. Vigabatrin for Oral Solution - recalled due to malfunction, USA

2 years ago •source fda.gov • details

Cipla Limited today announced that its wholly-owned subsidiary, InvaGen Pharmaceuticals Inc. is voluntarily recalling one lot of Vigabatrin for Oral Solution, USP 500mg, to the consumer level. Vigabatrin for Oral Solution, USP 500 mg has been found to have seal integrity issues allowing for powder leakage from… See more

#recall #drugs #unitedstates

Recalls InvaGen Pharmaceuticals Inc. Vigabatrin for Oral Solution - recalled due to malfunction Cipla Limite... photo #1
312   Comments Comment

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