The Recall Desk

State

Tennessee product recalls

73,495 recalls have nationwide distribution and so reach Tennessee. 7,853 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total
7,853
Critical
1,327
Severe
1,970
Most recent
2026-10-14

Of the 7,853 recalls naming Tennessee we have scored against our rubric, 1,327 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,970 (25%) are Severe.

Which agencies issued them

These figures cover only the 7,853 recalls whose distribution notice names Tennessee specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21851–21875 of 81348

  • SevereFDA (Devices)·Z-1320-2022·2022-07-13

    Dialysis Catheters Recalled for Potential Fluid Leakage from Hub Defect

    Covidien is recalling Mahurkar Chronic Carbothane dialysis catheters due to a potential leaking condition in the hub that may cause unanticipated fluid return during use. Approximately 132,443 units distributed worldwide are affected.

    Product
    Mahurkar Chronic Carbothane (Maxid) Catheter, Sterile, Single Use, Rx Only. For acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1314-2022·2022-07-13

    Palindrome Precision SI Chronic Catheters Recalled for Potential Hub Leaking

    Covidien recalls Palindrome Precision SI chronic dialysis catheters due to a potential leaking condition in the hub that may cause unanticipated fluid return during use.

    Product
    Palindrome Precision SI Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic hemodialysis, apheresis, and infusion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1341-2022·2022-07-13

    Cardiac Troponin Diagnostic Test Recalled for Positive Bias in Plasma Samples

    Siemens Dimension CTNI cardiac troponin test is recalled for positive bias (falsely elevated readings) in Lithium Heparin plasma samples, which may lead to misdiagnosis of myocardial infarction.

    Product
    Dimension CTNI-In vitro diagnostic test intended to quantitively measure cardiac troponin-I levels in human serum and heparinized plasma to aid in the diagnosis of myocardial infarction. Siemens Material Number (SMN)/REF (Catalog Number): 10444905/RF421C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1311-2022·2022-07-13

    NaturaLyte 2301 dialysate recalled for storage exposure and leaks

    Fresenius Medical Care recalled NaturaLyte 2301 dialysate in Texas and Louisiana after exposure to below-recommended storage temperatures. The exposure may cause packaging leaks, potentially leading to biological contamination and bloodstream infection risk.

    Product
    NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal, Model No. 08-2301-3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1407-2022·2022-07-13

    Plant-Based Yogurt Recall for Potential Glass Contamination

    EAT REAL FOOD LLC is recalling Culina Plant Based Yogurt nationwide due to potential glass fragments in the product. Affected units were distributed to all states.

    Product
    Plant Based Yogurt Culina Plain & Simple Nt Wt 5 oz. (142 g) UPC 854724007087 packaged in glass container 12 jars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1330-2022·2022-07-13

    Ossur Variflex Suba Junior prosthetic foot may crack under impact

    Ossur has recalled 410 Variflex Suba Junior prosthetic feet due to cracking and breaking under impact stress. The device is designed for children and adolescents worldwide.

    Product
    OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis, sized for children and adolescents.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1405-2022·2022-07-13

    Plant-Based Yogurt Recalled Due to Potential Glass Contamination

    EAT REAL FOOD LLC is recalling Culina Plant Based Blueberry Lavender Yogurt due to potential glass fragments. Affected lots were distributed nationwide with best-by dates in October and November 2022.

    Product
    Plant Based Yogurt Culina Blueberry Lavender Nt Wt 5 oz. (142 g) UPC 854724007117 packaged in glass container 12 jars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1410-2022·2022-07-13

    Plant-based yogurt recalled due to potential glass contamination

    EAT REAL FOOD LLC is recalling Plant Based Yogurt Culina Mango Orange Blossom due to potential glass contamination. The affected lot code is 07422CBCUCYMOB0723 with best-by date 11/13/2022, distributed nationwide.

    Product
    Plant Based Yogurt Culina Mango Orange Blossom Nt Wt 5 oz. (142 g) UPC 854724007230 packaged in glass container 12 jars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1406-2022·2022-07-13

    Plant Based Yogurt Recall Due to Potential Glass Contamination

    EAT REAL FOOD LLC is recalling Plant Based Yogurt Culina Bourbon Vanilla in 5 oz. glass jars nationwide due to potential glass fragments in the product. Consumers should not consume products with the affected lot codes.

    Product
    Plant Based Yogurt Culina Bourbon Vanilla Nt Wt 5 oz. (142 g) UPC 854724007094 packaged in glass container 12 jars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1338-2022·2022-07-13

    Rayner RayOne Intraocular Lens Systems Mislabeled with Incorrect Lens Strength

    Rayner is recalling RayOne intraocular lens injection systems because the outer package is mislabeled and contains a different lens strength than indicated. Approximately 162 devices were distributed in 13 US states.

    Product
    RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one MICS injection system with Intraocular Lens: (1) Outer carton labeled as Rayner RayOne EMV US, REF RAO200E, SE: +19.00D, Sph: +19.00D; and (2) Inner primary device packaging labeled as Rayner RayOne…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1408-2022·2022-07-13

    Plant-Based Strawberry Rose Yogurt Recalled for Potential Glass

    Culina Strawberry Rose plant-based yogurt is being recalled because glass may be present in the product. The recall affects 13,725 cases distributed nationwide.

    Product
    Plant Based Yogurt Culina Strawberry Rose Nt Wt 5 oz. (142 g) UPC 854724007100 packaged in glass container 12 jars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1321-2022·2022-07-13

    ABL800 Flex Analyzer Recalled for Potential Measurement Bias

    Radiometer Medical is recalling ABL800 Flex Analyzers that may produce biased measurements in sodium, calcium, and potassium levels. Approximately 1,489 analyzers are affected worldwide.

    Product
    ABL800 Flex Analyzer Model Numbers 393-800 and 393-801
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1409-2022·2022-07-13

    Plant-Based Yogurt Recalled for Potential Glass Contamination

    EAT REAL FOOD LLC is recalling Plant Based Yogurt Culina Peach Cashew due to potential glass contamination. The product was distributed nationwide in 13,725 cases.

    Product
    Plant Based Yogurt Culina Peach Cashew Nt Wt 5 oz. (142 g) UPC854724007254 packaged in glass container 12 jars per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1322-2022·2022-07-13

    EEA Autosuture Circular Staplers Recalled for Staple Guide Detachment Risk

    Covidien is recalling EEA Autosuture Circular Staplers (25mm) because the staple guide may not be securely attached and could disengage during use, potentially allowing the device to cut tissue without forming staples.

    Product
    EEA Autosuture Circular Stapler with DST Series Technology, 25mm. Model Numbers EEA25, EEAXL25, EEA2535, and EEAXL2535.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1184-2022·2022-07-13

    Boric Acid Vaginal Suppositories Recalled Due to Manufacturing Control Defects

    Wedgewood Village Pharmacy is recalling Boric Acid 600 mg vaginal suppositories (Lot #000-03843532) nationwide due to insanitary manufacturing conditions and lack of processing controls detected during an FDA inspection. No illnesses have been reported.

    Product
    Boric Acid 600 mg per suppository, 14 Vaginal Suppositories per box, Wedgewood Village Pharmacy LLC, 405 Heron Drive, Ste 200, Swedesboro, NJ 08085
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1344-2022·2022-07-13

    Abbott TactiCath Ablation Catheter System Error Display Malfunction

    Abbott recalls 191 TactiCath cardiac ablation catheters that may display incorrect error messages when connected to the EnSite Precision Navigation System, potentially causing user confusion.

    Product
    Abbott TactiCath Sensor Enabled, Contact Force Ablation Catheter, 8F 115cm FJ, REF A-TCSE-FJ. For mapping of the heart chambers during ablation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1339-2022·2022-07-13

    Imaging system software displays mirrored CT images during data loading

    Siemens imaging systems with syngo VE20 software may display CT images mirrored horizontally and vertically when loading Toshiba data, potentially causing misinterpretation of patient positioning and inappropriate treatment.

    Product
    syngo Application software VE20 (Material Number 10848815) installed on the Artis pheno and Artis icono systems as follows: (1) Artis pheno Model Number:10849000 (2) Artis icono biplane Model Number: 11327600 (3) Artis icono floor Model Number: 11327700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1335-2022·2022-07-13

    VERIGENE Enteric Pathogens Test may yield false negative results

    Luminex Corporation is recalling VERIGENE Enteric Pathogens tests worldwide due to potential false negative results caused by hydrophobic characteristics of the sampling swab. The defect could lead to missed detection of infections in stool specimens.

    Product
    VERIGENE Enteric Pathogens Nucleic Acid Test, Part No. 30-002-23
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1186-2022·2022-07-13

    Estriol Vaginal Cream Recalled Due to Insanitary Manufacturing Conditions

    Wedgewood Village Pharmacy is recalling Estriol vaginal cream nationwide due to insanitary manufacturing conditions and lack of processing controls identified during an FDA inspection.

    Product
    Estriol 1mg/gm, Vaginal Cream, 60 gm tube, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Drive, Ste 200, Swedesboro, NJ 08085
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1331-2022·2022-07-13

    Omnera 400T Radiographic System Recalled for Potential Overhead Crane Malfunction

    Arcoma AB is recalling 71 Omnera 400T radiographic systems because liquid ingress in the display handles may cause electrical short circuits and uncontrolled movement of the overhead tube crane.

    Product
    Omnera 400T Digital Radiographic System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1332-2022·2022-07-13

    Omnera 400A Digital Radiographic System: Electrical Short Circuit Hazard

    Arcoma AB recalls 47 Omnera 400A Digital Radiographic Systems due to potential electrical short circuits that could cause uncontrolled movement of the overhead tube crane.

    Product
    Omnera 400A Digital Radiographic System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1185-2022·2022-07-13

    Estriol Vaginal Cream Recalled for Insanitary Manufacturing Conditions

    Wedgewood Village Pharmacy is recalling Estriol 1mg/gm Vaginal Cream due to insanitary manufacturing conditions and lack of adequate processing controls identified during FDA inspection. The product was distributed nationwide.

    Product
    Estriol 1mg/gm, Vaginal Cream, 30 gm tube, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Drive, Ste 200, Swedesboro, NJ 08085
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1340-2022·2022-07-13

    Siemens Dimension LTNI Cardiac Troponin Test Positive Bias Recall

    Siemens is recalling the Dimension LTNI cardiac troponin-I test due to positive bias in Lithium Heparin plasma samples, which may cause false-positive results and inappropriate medical intervention.

    Product
    Dimension LTNI -In vitro diagnostic test intended to quantitively measure cardiac troponin-I levels in human serum and heparinized plasma to aid in the diagnosis of myocardial infarction. Siemens Material Number (SMN)/REF (Catalog Number): 10444896/RF521
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1183-2022·2022-07-13

    Boric Acid 600 mg Capsules Recalled for Insanitary Manufacturing Conditions

    The FDA has recalled Boric Acid 600 mg capsules (Lot #000-03868160, Exp: 09/14/22) manufactured by Wedgewood Village Pharmacy due to insanitary conditions and lack of processing controls observed during FDA inspection. The recalled product was distributed nationwide.

    Product
    Boric Acid 600 mg capsules, 14 capsules per box, Qty: 1, Wedgewood Village Pharmacy LLC, 405 Heron Drive, Ste 200, Swedesboro, NJ 08085
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1343-2022·2022-07-13

    Fluoroscopic X-Ray System Stand Movement May Be Blocked During Use

    Siemens Artis and Artis Q.zeego fluoroscopic X-ray systems may lose stand mobility if the robotic control system's BIOS battery discharges at startup. Field service is required to restore function.

    Product
    Artis zeego (Model no. 10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System
    Category
    Medical Device
    Distribution
    Distributed nationwide