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Safety Reports: Recall

Updated:

Baxter International Inc. announced today it has issued an Urgent Medical Device Correction for Spectrum V8 and Spectrum IQ infusion pumps in the U.S. and Puerto Rico that have been upgraded to software versions v8.01.01 and v9.02.01. The Correction is due to an increase in reported false… See more

#medicaldevices #recall #unitedstates

FDA announced the recall of 184 containers of Uneviscerated whole dried sardines used in raw pet food by What The Raw due to potential Clostridium botulinum contamination. This product was distributed to retail locations in Ohio (in 2022 and 2023) and Pennsylvania (in 2021 and 2022).

The… See more

#petfood #recall #unitedstates #botulism

The Arizona Department of Health Services (ADHS) announced the recall of Divinity and MAC from Grow Sciences and Gelato 41 from Soothing Options due to possible contamination with Aspergillus, a fungus that can cause allergic reactions or infection, usually in people already sick with something else. To… See more

#recall #arizona #unitedstates

FDA announced the recall of 1st phorm Level-1 Sustained Assimilation Protein Supplements Chocolate Marshmallow and Milk Chocolate flavors by International Food Companies DBA because they may be contaminated with Staphylococcus aureus bacteria. These products were distributed in Missouri.

The recalled products are:
- 1st phorm Level-1 Sustained… See more

#recall #missouri #unitedstates #staphylococcus

Sci-Mx Nutrition is extending their recall of Sci-Mx Nutrition Ultra Muscle Strawberry Flavour sold at Home Bargains because high levels of caffeine have been found in the product. This makes the product unsafe to consume. Some of these products were found to contain levels of caffeine at… See more

#recall #unitedkingdom

Tillomed Laboratories Limited is recalling one batch of Labetalol 200mg Tablets due to an error on the foil blister packaging. The incorrect aluminium foil blister packaging states Labetalol 100mg Tablets, however it should be labelled as Labetalol 200mg Tablets. This error has occurred at the primary packing… See more

#recall #drugs #unitedkingdom

Cipla Limited (BSE: 500087; NSE: CIPLA EQ; and hereafter referred to as "Cipla"), today announced that its wholly-owned subsidiary Cipla US is voluntarily recalling six batches of Albuterol Sulfate Inhalation Aerosol, 90 mcg (200 Metered Inhalation) manufactured in November 2021 to the consumer level due to Failure… See more

#drugs #recall #unitedstates

Home Bargains is recalling Sci-Mx Nutrition Ultra Muscle Strawberry Flavour because high levels of caffeine have been found in the product. This makes the product unsafe to consume.

-Product details
Sci-Mx Nutrition Ultra Muscle Strawberry Flavour, Pack size: (1.5kg bags), Batch code: W110429, Best before: March 2025… See more

#recall #unitedkingdom

FDA announced the recall of 6,777 bottles of VIT-RA-TOX Calphonite #38 and Sonne's Calphonite #2 by Anatox Inc due to Elevated lead levels. These products were distributed to Distributors, retailers, and consumers in AL, AZ, CA, CT, CO, FL, GA, IL, IN, KS, KY, MA, MD, MN,… See more

#recall #unitedstates

Sonne's Detoxificant #7 - recalled due to Elevated lead levels, USA

1 year ago source accessdata.fda.gov details

Recall notice

FDA announced the recall of 2,870 bottles of Sonne's Detoxificant #7 by Anatox Inc due to Elevated lead levels. These products were distributed to distributors, retailers, and consumers in AL, AZ, CA, CT, CO, FL, GA, IL, IN, KS, KY, MA, MD, MN, MO, NC, NM, NY,… See more

#recall #unitedstates