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Archives

TruLaw FDA Warning Image

According to the FDA, a recall of GE HealthCare’s Nuclear Medicine 600/800 Series systems has been identified as Class I due to a potential product defect and missing part that could result in serious injury or death. Indicated for use by healthcare professionals to assess […]

Feb 16, 2023 By TruLaw

FDA Alerts – Class I recall of Nuclear Medicine 600/800 Series systems by GE HealthCare due to missing parts

TruLaw FDA Warning Image

Volt Candy, of Pomona, California, has voluntarily recalled one lot of its PrimeZen Black 6000 capsules at the consumer level after an FDA analysis yielded traces of undeclared sildenafil and tadalafil in the product. As phosphodiesterase (PDE-5) inhibitors typically present in FDA-approved male erectile dysfunction […]

Feb 15, 2023 By TruLaw

FDA Alerts – PrimeZen Black 6000 capsules by Volt Candy recalled due to undeclared sildenafil, tadalafil

TruLaw FDA Warning Image

In an updated communication posted on February 7, 2023, the FDA is alerting patients that Guttenberg, New Jersey-based Advanced Women Imaging has had its Mammography Quality Standards Act (MQSA) certificate revoked until January 4, 2025. The loss of accreditation means the facility can no longer […]

Feb 13, 2023 By TruLaw

FDA Alerts – Advanced Women Imaging, operators lose Mammography Quality Standards Act (MQSA) accreditation until Jan. 2025

TruLaw FDA Warning Image

In an allergy alert issued on February 4, 2023, Titans Global Inc indicated it was recalling its “JSJ Chocolate Cake,” “JSJ ZSR Cake,” and “JSJ DMC Leaf Cake” because the ingredient list printed on all product labeling does not declare egg as a possible allergen. […]

Feb 10, 2023 By TruLaw

FDA Warns – “JSJ Chocolate Cake,” “JSJ ZSR Cake,” and “JSJ DMC Leaf Cake” recalled by Titans Global Inc due to undeclared egg

TruLaw FDA Warning Image

In a February 8, 2023 update to a safety communication regarding a Class I recall of the Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test, the FDA has named Universal Meditech Inc. as another distributor of the unapproved product. Originally issued on May 10, 2022, the […]

Feb 9, 2023 By TruLaw

FDA Alerts – Class I recall of Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test updated to include additional distributor

TruLaw FDA Warning Image

According to the FDA, a recall of CADD System Administration Sets and Cassette Reservoirs by Smiths Medical has been identified as Class I due to issues that may cause major injuries or death. Disposable and intended for use with CADD infusion pumps, the CADD Administration […]

Feb 8, 2023 By TruLaw

FDA Warns – Class I recall of CADD Infusion System Administration Sets and Cassette Reservoirs by Smiths Medical due to product defects

TruLaw FDA Warning Image

According to the FDA, Baltimore, Maryland-based Fresh Ideation Food Group LLC has initiated a recall of hundreds of ready-to-eat sandwiches and other food products under multiple brands. A press release on February 3, 2023, indicates the company took action after environmental sampling in its facilities […]

Feb 7, 2023 By TruLaw

FDA Alerts – Hundreds of ready-to-eat sandwiches, other products recalled by Fresh Ideation Food Group LLC due to potential Listeria contamination

TruLaw FDA Warning Image

The FDA is calling to attention a voluntary recall to the consumer level of Artificial Tears Lubricant Eye Drops by Global Health Pharma Healthcare due to potential contamination. The company announced the action on February 2, 2023, after the FDA was notified by the Centers […]

Feb 7, 2023 By TruLaw

FDA Warns – Global Health Pharma Healthcare recalls Artificial Tears Lubricant Eye Drops distributed by EzriCare & Delsam Pharma

TruLaw FDA Warning Image

Herndon, Virginia-based Shop Me Ca has voluntarily recalled its “Diep Bao Cream,” a baby skin cream, after testing by Oregon Health Authority (OHA) detected high lead levels in two samples, according to the FDA. The action was initiated on February 1, 2023, after the company […]

Feb 3, 2023 By TruLaw

FDA Alerts – “Diep Bao Cream” by Shop Me Ca recalled due to potential lead contamination

TruLaw FDA Warning Image

According to the FDA, Philips Respironics has recalled several masks for BiPAP and CPAP machines after officials learned the magnetic clips used to hold them in place could cause potential injury or death. The FDA initiated the action on August 2, 2022, and impacts masks […]

Feb 2, 2023 By TruLaw

FDA Alerts – Philips Respironics issues Class I recall of multiple masks for BiPAP, CPAP machines due to danger posed by magnetic clips

TruLaw FDA Warning Image

Lakewood, Washington-based Joy Joy’s Bakery has recalled its Ube Spanish Bread, Ube Ensaymada, and Ube Roll due to inadequate disclosure of wheat allergen on product labels, according to the FDA. The action was initiated on January 26, 2023, after the Oregon Department of Agriculture, by […]

Feb 1, 2023 By TruLaw

FDA Warns – Joy Joy’s Bakery recalls Ube Spanish Bread, Ube Ensaymada, and Ube Roll due to undeclared wheat

The FDA is alerting consumers to an important update of a July 29, 2022 recall of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 by Edgewell Personal Care due to trace levels of benzene. On January 27, 2023, Edgewell Personal Care announced another batch […]

Jan 31, 2023 By TruLaw

FDA Alert – Expanded recall of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 by Edgewell Personal Care

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