All recall categories

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 48,122 notices were distributed nationwide, so they reach Tennessee too — those are in the archive.

Medical devices

Reported Sep 12, 2018

Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive Sleep Apnea, Inspire Part #900-003-020, Product…

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

Inspire Medical Systems Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 12, 2018

El Guapo Jamaica Hibiscus Flowers in flexible pouches , 1 oz., 2 oz., 8 oz., 16 oz., and 10 lb. box .

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

Mojave Foods Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 12, 2018

Outer Package Label: Tapered Screw-Vent Implant System, 4.1mm X 10mm, 3.5mm, REF:TSVM4B10, Sterile:R, Rx Only; Inner…

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

Zimmer Dental Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 5, 2018

Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product Packaging: Three (3) PVP-I prep pads…

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

Bard Medical Division

FDA (openFDA device enforcement)

Medical devices

Reported Sep 5, 2018

FLOSEAL Special Applicator Tips in cartons labeled in part, "Floseal SPECIAL APPLICATOR TIPS***6 x Malleable Tip…

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

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 5, 2018

Premo Brand Turkey & Cheese Wedge sandwiches 5 OZ retail UPC 612510002018 Plastic triangle sandwich wedge container…

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

Lipari Foods Operating Company, LLC dba JLM Manufacturing

FDA (openFDA food enforcement)

Medical devices

Reported Sep 5, 2018

Verigene Enteric Pathogens Nucleic Acid Test (EP) for detecting and identification of pathogenic enteric bacteria,…

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

Luminex Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 5, 2018

Stryker Mako Vizadisc Knee Procedure Tracking Kit

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

Mako Surgical Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 5, 2018

Medline 0.9 % Sodium Chloride Injection, USP 5 mL in 10 mL Syringe ZR Intended for flushing IV catheters and IV tubing…

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

Medline Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent…

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

Biomerieux Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a. CMI-0100 PNX, Pro-Nox Mixer - Canadian; b.…

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

CAREstream Medical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

CPAP Mask Cushion, Model Nos. PB781S, PB781M, PB781L, 781S, 781M and 781L Product Usage: A CPAP mask is attached to an…

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

Compass Health Brands (Corporate Office)

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

BEST TASTE BRAND SNACK GINGER SLICED, Net Weight 200g, 7 OZ, Distributed by; COUNTRY FAVOR., INC U.S.A; PRODUCT OF…

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

Country Favor Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 29, 2018

Dole Classic Coleslaw, 14 oz. (397 g) plastic bag; Green Cabbage, shredded carrots. UPC Code 7143001066 Distributed by…

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

Dole Fresh Vegetables Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise…

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

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body,…

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

GE Healthcare Japan Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

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

Handicare USA Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12…

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

Johnson & Johnson Vision Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or…

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

Liebel-Flarsheim Company LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

Peanut Paste/Butter bulk tankers

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

Peanut Processors, Inc.

FDA (openFDA food enforcement)

Food

Reported Aug 29, 2018

Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. container, or 3…

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

Salt & Straw LLC

FDA (openFDA food enforcement)

Meat & poultry

Reported Aug 29, 2018

Taylor Farms Illinois, Inc. Retira Productos De Pastel De Carne Y Cerdo Debido A Errores De Rotulacin Y Alrgenos No…

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

Taylor Farms Illinois, Inc.

USDA FSIS

Medical devices

Reported Aug 22, 2018

Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band system consists of a silicone band with…

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

Apollo Endosurgery Inc.

FDA (openFDA device 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.