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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

B. Braun Medical Inc. 0.9% Sodium Chloride for Injection USP 250ML in Excel - recalled due to Fluid Leakage, USA

4 years ago •source fda.gov • details

B. Braun Medical Inc. (B. Braun) is voluntarily recalling five (5) lots of 0.9% Sodium Chloride for Injection USP 250ML in Excel within the United States to the hospital/user level. The biggest risk with a slow leak in any intravenous solution preparation is a break in sterility… See more

#drugs #recall #blood #unitedstates #pita #ro-tel

Recalls B. Braun Medical Inc. 0.9% Sodium Chloride for Injection USP 250ML in Excel - recalled due to Fluid... photo #1
312   Comments Comment

Recall notice

Family Dollar Drugs, Medical Devices, Cosmetics, & Food products - recalled due to Salmonella and rodent contamination, USA

4 years ago •source fda.gov • details

Family Dollar, Inc. is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and shipped to 404 stores from Family Dollar Distribution Center 202 in West Memphis, Arkansas from January 1, 2021 through the… See more

#dogfood #familydollar #catfood #petfood #recall #drugs #medicaldevices #rodents #rats #mice #unitedstates #applegate #arnold

Recalls Family Dollar Drugs, Medical Devices, Cosmetics, & Food products - recalled due to Salmonella and ro... photo #1
  Comments Comment

Recall notice

Dogs Choice UK frozen raw dog foods - recalled due to the presence of Salmonella, England, UK

4 years ago •source data.food.gov.uk • details

Dogs Choice UK is recalling a number of frozen raw dog foods because Salmonella has been found in the products.

- Frozen Chicken and Beef (500g). Batch code: 080222+2. Best before: 08 August 2022
- Frozen Chicken and Beef Ready Meal (500g). Batch code: 080222+2. Best before:… See more

#dogfood #recall #frozenfood #petfood #raw #england #unitedkingdom #beef #chicken

Recalls Dogs Choice UK frozen raw dog foods - recalled due to the presence of Salmonella Dogs Choice UK is r... photo #1
79   Comments Comment

Recall notice

Spectrum V8 and Spectrum IQ infusion pumps - recalled due to alarm malfunction, USA

4 years ago •source fda.gov • details

Baxter International Inc. announced today it has issued an Urgent Safety Communication to reinforce important safety information regarding upstream occlusion alarms for all Spectrum V8 and Spectrum IQ infusion pumps. Incorrect administration set setup and/or incomplete resolution of upstream occlusion alarms may result in reduced delivery or… See more

#recall #medicaldevices #unitedstates #ham #bean #roll #ro-tel

312   Comments Comment

Recall notice

Red Mammoth capsules - recalled due to Undeclared Sildenafil and Tadalafil, USA

4 years ago •source fda.gov • details

Celebrate Today is voluntarily recalling lot number DK1027, Exp 08/01/2023 of Red Mammoth capsules to the consumer level. Celebrate Today was informed by Amazon that laboratory analysis has found the product to be tainted with sildenafil and tadalafil To date, Celebrate Today has not received any reports… See more

#drugs #recall #blood #unitedstates

Recalls Red Mammoth capsules - recalled due to Undeclared Sildenafil and Tadalafil Celebrate Today is volunt... photo #1
312   Comments Comment

Recall notice

Red Mammoth Capsules - recalled due to undeclared Sildenafil and Tadalafil, USA

4 years ago •source fda.gov • details

Celebrate Today is voluntarily recalling lot number DK1027, Exp 08/01/2023 of Red Mammoth capsules to the consumer level. Celebrate Today was informed by Amazon that laboratory analysis has found the product to be tainted with sildenafil and tadalafil, ingredients known as phosphodiesterase (PDE-5) inhibitors found in FDA… See more

#vitamins #recall #blood #unitedstates

Recalls Red Mammoth Capsules - recalled due to undeclared Sildenafil and Tadalafil Celebrate Today is volunt... photo #1
312   Comments Comment

Recall notice

MAC DADDY DIETARY SUPPLEMENTS - recalled due to undeclared Sildenafil & Tadalafil, USA

4 years ago •source fda.gov • details

ABC SALES 1 INC is voluntarily recalling MAC DADDY RED Capsules, Lot 1230004, Exp 03/30/2024 and MAC DADDY PURPLE Capsules, Lot 1230005, Exp 03/30/2024 to the consumer level. ABC Sales 1 Inc was informed by Amazon that laboratory analysis found MAC DADDY RED capsules to be tainted… See more

#drugs #recall #blood #unitedstates

Recalls MAC DADDY DIETARY SUPPLEMENTS - recalled due to undeclared Sildenafil & Tadalafil ABC SALES 1 INC is... photo #1
312   Comments Comment

Recall notice

Your Favorite Shop The Red Pill - recalled due to undeclared Tadalafil, USA

4 years ago •source fda.gov • details

Your Favorite Shop is voluntarily recalling lot # 26436989. Expiry 10/30/2023 of The Red Pill, packaged in 10-count blisters packaged in a carton to the consumer level. The product was distributed via the internet and fulfilled by Amazon at www.amazon.com nationwide in the USA.

Your Favorite Shop… See more

#blood #drugs #recall #unitedstates

Recalls Your Favorite Shop The Red Pill - recalled due to undeclared Tadalafil Your Favorite Shop is volunta... photo #1
312   Comments Comment

Recall notice

STANDARD Q COVID-19 Ag Home Test - recalled due to illegally imported into the US, USA

4 years ago •source fda.gov • details

SD Biosensor, Inc., a global in-vitro diagnostics company, is voluntarily recalling its STANDARD Q COVID-19 Ag Home Test in the United States, due to confirmed reports that the test kits were illegally imported into the United States. The STANDARD Q COVID-19 Ag Home Test is not authorized,… See more

#medicaldevices #recall #unitedstates

Recalls STANDARD Q COVID-19 Ag Home Test - recalled due to illegally imported into the US SD Biosensor, Inc.... photo #1
313   Comments Comment

Recall notice

Vyaire Medical ventilators - recalled due technical failure alarm, USA

4 years ago •source fda.gov • details

Imtmedical ag, a subsidiary of Vyaire Medical, initiated a voluntary field correction for certain bellavista™ ventilators. With specific software version and configuration combinations, the ventilators can cease ventilation and generate a technical failure alarm 305. There is a potential issue with bellavista™ 1000 and 1000e ventilators that… See more

#medicaldevices #recall #unitedstates

Recalls Vyaire Medical ventilators - recalled due technical failure alarm Imtmedical ag, a subsidiary of Vya... photo #1
312   Comments Comment

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