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Recalls distributed in Tennessee

These notices name Tennessee in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,181 stored notices name Tennessee, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Tennessee too — those are in the archive.

Medical devices

Reported Feb 3, 2021

Brain Heart Infusion Agar with 6 ug/ml Vancomycin Cat no: G14 Lot no: 472698 Manufactured: 2020-10-29 Expires:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hardy Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Feb 3, 2021

PSG-1100 Sleep Diagnostic System. Sample product label: JB-110A SERIAL No. 01454 RoHS Compliant; PSG-100 Head Box; UDI…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nihon Kohden America Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 3, 2021

Blueberry Blizzard Coffee Cake, Item 259, Net Wt. 24 oz.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nueske Applewood Smoked Meat, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 3, 2021

O H Danish Bakery Almond Danish Kringle, UPC 67209-00006. Net Weight: 24 oz. (1 lb. 8 oz) 680.3 grams

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

O & H Danish Bakery

FDA (openFDA food enforcement)

Medical devices

Reported Feb 3, 2021

Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Respironics California, LLC

32 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 3, 2021

Cardiovascular Reprocessed ViewFlex Xtra ICE Catheter, REF D087031, OM St. Jude Medical, Size 9F (3.2mm), Length 90 cm,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Food

Reported Jan 27, 2021

JTM FOOD GROUP brand READY TO EAT WHITE CHEDDAR MACARONI & CHEESE in 5 lb. plastic bags, 6 bags per case.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

JTM Provisions Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 27, 2021

REF 27219-1 X1, Medtronic, Delta Valve, Neonatal, Performance Level 1.0, CE 0344, Sterile EO - Product Usage: Neonatal…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Neurosurgery

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 27, 2021

Penumbra JET 7 Reperfusion Catheter REF 5MAXJET7 The Penumbra JET 7 Reperfusion Catheter with Xtra Flex technology (JET…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Penumbra Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 27, 2021

FITNESS LABS***Organic***Coconut Oil***Extra Virgin***16 fl. oz. (473 mL)***Carefully Designed and Distributed by…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Piping Rock Health Products

FDA (openFDA food enforcement)

Medical devices

Reported Jan 27, 2021

Portex Acapella DH Vibratory PEP Device - Product Usage: a single patient use device that provides Positive Expiratory…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2021

Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, sterile, REF…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Boston Scientific Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2021

icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended for patients for whom the monitoring of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2021

All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC 7C, EPIQ 7W, EPIQ…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2021

Remel Blood Agar/MacConkey Agar Bi-Plate, REF: R02049

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remel Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 13, 2021

Backroad Country Spicy Cajun Mix 9 oz (255g) plastic bag. Packed by Troyer Manufacturing Millersburg, OH 44654.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lipari Foods Operating Company, LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 13, 2021

Bone fixation nail. TRIGEN INTERTAN - Product Usage: indicated for fractures of the femur including simple shaft…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

APEX Compounding System Control Panel Module, REF: 601224, Product Code AX1000 - Product Usage: intended for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

B Braun Medical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

MicroScan Pos MIC Panel Type 34 - Product Usage: For the determination of antimicrobial agent susceptibility and/or…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

Flexor Check-Flo Introducer, RPN KCFW-4.0-35-55-RB-HFANL0-HC, Order Number G56229 Flexor Introducers and Guiding…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cook Inc.

20 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

Viral Transport Medium, 3ml, Ref: R99, Container type: Tube, Packaged: 20 tubes/box, IVD, CVM Transport Media is…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hardy Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

42 IN (107 cm) Appx 5.0 ml, 20 Drop Admin Set, Spiros, REF: 20131-01; 31" (79 cm) Admin Set w/20 Drop Integrated Clave…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2020

Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nova Ortho-Med Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 30, 2020

Organic fresh cut basil packaged in plastic clamshell containers The Fresh Market Organic Basil NET WT 0.5oz (14g),…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Shenandoah Growers, Inc.

FDA (openFDA food enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.