Department of JusticeU.S. Attorney’s OfficeDistrict of Kansas FOR IMMEDIATE RELEASEWednesday, February 16, 2022 KANSAS CITY, KAN. – A federal grand jury in Kansas City returned an indictment charging a pharmacist with one count of tampering with a consumer product, one count of possession of Tramadol by deception and subterfuge, one count of possession of Zolpidem…
Golden Medal Mushroom Inc. Recalls Enoki Mushrooms Because of Possible Health Risk (Revised)
Summary Company Announcement Date: February 23, 2022 FDA Publish Date: February 25, 2022 Product Type: Food & Beverages Produce Foodborne Illness Reason for Announcement: Recall Reason Description Listeria Monocytogenes Company Name: Golden Medal Mushroom Inc. Brand Name: Brand Name(s) Golden Medal Mushroom Inc. Product Description: Product Description Enoki Mushrooms Company Announcement Golden Medal Mushroom Inc….
Dried Plums Recall Information
Summary Company Announcement Date: February 15, 2022 FDA Publish Date: February 24, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description potential to be contaminated with lead Company Name: Alli and Rose LLC Brand Name: Brand Name(s) Product Description: Product Description Dried Plums/ saladitos Company Announcement IDENTIFYING FEATURESBarcode: 810019600821Item code: 1516905 Dates…
Arrow International, LLC (Subsidiary of Teleflex Inc.) Recalls the Arrow-Trerotola Percutaneous Thrombolytic Device Due to Risk of Tip Damage During Use
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Names: Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Model Number: See Recall Database Entry Manufacturing Dates: January 1, 2020 to December 31, 2021 Distribution Dates: February 1, 2020…
Pharmacist Admits Prescription Drug Theft and Tampering
Department of JusticeU.S. Attorney’s OfficeNorthern District of Iowa FOR IMMEDIATE RELEASEWednesday, February 23, 2022 A pharmacist who stole controlled substances from two Dubuque area pharmacies and tampered with medications pled guilty yesterday in federal court in Cedar Rapids. Anthony Pape, age 33, from Dubuque, Iowa, was convicted of two counts of theft of controlled substances…
Vadilal Industries (USA) Recalls “Custard Apple Pulp” Because of Possible Health Risk
Summary Company Announcement Date: February 22, 2022 FDA Publish Date: February 22, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Salmonella Company Name: Vadilal Industries Inc. Brand Name: Brand Name(s) Product Description: Product Description frozen custard apple pulp Company Announcement Vadilal Industries (USA) Inc. of Newark, NJ is voluntarily recalling two…
BASE10 Genetics Recalls RNAstill MTM Specimen Collection Kits That Are Not Authorized, Cleared, or Approved by the FDA, May Give False Results, and Require Special Training for Safe Handling
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Name: RNAstill MTM specimen collection kits Product Codes: See Recall Database Entry Distribution Dates: September 16, 2020 to December 1, 2021 Devices Recalled in the U.S.:…
E25Bio Recalls COVID-19 Direct Antigen Rapid Tests That Are Not Authorized, Cleared, or Approved by the FDA and May Give False Results
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product (Include the following information) Product Names: E25Bio COVID-19 Direct Antigen Rapid Test; Trade Name: E25Bio SARS-CoV-2 Antigen Test Kit Product Codes and Model Numbers: See Recall Database…
Family Dollar Stores Issues Voluntary Recall of Certain FDA-Regulated Products in Six States Including Drugs, Devices, Cosmetics, Foods
Summary Company Announcement Date: February 18, 2022 FDA Publish Date: February 18, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Salmonella contamination and presence of rodent activity at the distribution center Company Name: Family Dollar, Inc. Brand Name: Brand Name(s) Numerous brand names Product Description: Product Description Numerous human food,…
Baxter Issues Urgent Safety Communication to Reinforce Important Safety Information Regarding Upstream Occlusion Alarms for all Spectrum V8 and Spectrum IQ Infusion Pumps
Summary Company Announcement Date: February 17, 2022 FDA Publish Date: February 18, 2022 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Potential for alarm malfunction Company Name: Baxter International Inc. Brand Name: Brand Name(s) SIGMA Spectrum V8 and Spectrum IQ Product Description: Product Description Spectrum V8 and Spectrum IQ infusion pumps Company Announcement…