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Safety Reports: Recall

Updated: December 20, 2023 11:01 AM

Real Time Reports

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

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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

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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

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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

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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

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Recall notice

Artri King, Kuka Flex Forte and Reumo Flex food supplements - recalled due to not permitted active ingredients, Ireland

2 years ago •source fsai.ie • details

The FSAI announced the recall of Artri King, Kuka Flex Forte, and Reumo Flex food supplements because they contain active ingredients not approved for use in food products and are not declared on the label. All three products contain the active ingredient diclofenac and Artri King also… See more

#recall #ireland

Recalls Artri King, Kuka Flex Forte and Reumo Flex food supplements - recalled due to not permitted active i... photo #1

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Recall notice

Kodiak Premium Wintergreen Longcut Smokeless Tobacco - recalled due to the presence of foreign metal objects, Alton, Kentucky 40342, USA

2 years ago •source fda.gov • details

American Snuff Company (ASC) is voluntarily recalling certain lots of Kodiak Premium Wintergreen Longcut Tobacco manufactured at ASCs facility in Clarksville, TN. ASC initiated the recall of Kodiak Premium Wintergreen Longcut Tobacco after having identified the potential for certain lots of the product to contain foreign metal… See more

#recall #tobacco #alton #kentucky #unitedstates

Recalls Kodiak Premium Wintergreen Longcut Smokeless Tobacco - recalled due to the presence of foreign metal... photo #1

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Recall notice

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

2 years ago •source fda.gov • details

In direct response to the 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… See more

#recall #medicaldevices #unitedstates

Recalls Covidien and Cardinal Health Urology and OR room specific kits and trays - recalled due to lack of s... photo #1

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Recall notice

Baxter Novum IQ syringe infusion pump - recalled due to malfunction, USA

2 years ago •source fda.gov • details

Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for the Novum IQ syringe infusion pump. The Correction is due to the potential for an incomplete infusion following one or more downstream occlusion alarms. Baxter notified impacted customers in October and is developing… See more

#recall #medicaldevices #unitedstates

Recalls Baxter Novum IQ syringe infusion pump - recalled due to malfunction Baxter International Inc. announ... photo #1

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Recall notice

Magnum Male Sexual Enhancement capsule - recalled due to undeclared sildenafil, USA

2 years ago •source fda.gov • details

Meta Herbal is voluntarily recalling 500 blister packs of Magnum XXL 9800 2000 mg per capsule, to the consumer level. The products have been found to be tainted with Sildenafil. Products containing sildenafil cannot be marketed as dietary supplements. Magnum XXL 9800 capsules is an unapproved new… See more

#drugs #recall #amazon #unitedstates

Recalls Magnum Male Sexual Enhancement capsule - recalled due to undeclared sildenafil Meta Herbal is volun... photo #1

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Safety Reports: Recall

Real Time Reports

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

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

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

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

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

Artri King, Kuka Flex Forte and Reumo Flex food supplements - recalled due to not permitted active ingredients, Ireland

Kodiak Premium Wintergreen Longcut Smokeless Tobacco - recalled due to the presence of foreign metal objects, Alton, Kentucky 40342, USA

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

Baxter Novum IQ syringe infusion pump - recalled due to malfunction, USA

Magnum Male Sexual Enhancement capsule - recalled due to undeclared sildenafil, USA

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