State

Tennessee product recalls

73,718 recalls have nationwide distribution and so reach Tennessee. 7,859 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,859
Critical: 1,324
Severe: 1,973
Most recent: 2026-10-28

Of the 7,859 recalls naming Tennessee we have scored against our rubric, 1,324 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,973 (25%) are Severe.

Which agencies issued them

These figures cover only the 7,859 recalls whose distribution notice names Tennessee specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

76–100 of 81577

ModerateFDA (Drugs)·D-0054-2027·2026-10-28
Pritam International Recalls Brush Buddies Fluoride Toothpaste for CGMP Deviations
Pritam International is voluntarily recalling 411,600 tubes of Brush Buddies Hot Wheels Anticavity Fluoride Toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Brush Buddies, Hot Wheels, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Strawberry Flavor, Net Wt. 4.0 oz (113g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-002-40, Item # 88047, UPC 8 10147 88047 8
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0194-2027·2026-10-28
Medtronic NDI Passive Spheres Recalled for Reflective Material Variation
Medtronic is recalling NDI Passive Spheres and biopsy needle kits because reflective material variation may affect the navigation system's ability to detect and track the spheres.
Product
Medtronic NDI Passive Spheres REF: 8801071, Sterile EO, 1/Tray 12 pk., Rxonly
Category
Medical Device
Distribution
52 states
ModerateFDA (Devices)·Z-0233-2027·2026-10-28
Boston Scientific Recalls Direxion Torqueable Microcatheters for Coating Defects
Boston Scientific is recalling 3,284 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/SWAN/1RO/130; Material Number: M001195300
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0066-2027·2026-10-28
Brush Buddies Toothpaste Recalled for Manufacturing Deviations
Pritam International is voluntarily recalling Brush Buddies toothpaste nationwide due to CGMP deviations. No illnesses or injuries are reported.
Product
BB (Brush Buddies) Cavity Protection, Anti-Cavity Fluoride Toothpaste, (sodium monofluorophosphate 0.76%) Cool Mint, 2 Value Pack, Two 3.5 oz (99g) tubes, Total Net Wt 7 oz (198g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-035-10, Item # 88543, UPC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0067-2027·2026-10-28
Pritam International Recalls Brush Buddies Toothpaste Due to CGMP Deviations
Pritam International is voluntarily recalling 198,288 tubes of Brush Buddies toothpaste nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Product
BB (Brush Buddies) Advanced Whitening, Anti-Cavity Fluoride Toothpaste, (sodium fluoride 0,24%) Peppermint, Net Wt 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-885-42, Item # 88542, UPC 8 10147 88542 8
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0276-2027·2026-10-28
Medline Medical Convenience Kits Recalled for Adhesive Removal Issues
Medline Industries is recalling 2,229 medical convenience kits because they are difficult to remove from patients and leave adhesive residue on the skin.
Product
MEDLINE medical convenience kits labeled as: 1) BIRTHDAY KIT-DOUBLE BASIN-LF, Medline Kit Number/SKU DYNJ16127N; 2) NYGH-DELIVERY PACK-LF, Medline Kit Number/SKU DYNJ27206D; 3) OB/GYN, Medline Kit Number/SKU DYNJ911652.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0231-2027·2026-10-28
Boston Scientific Recalls Direxion Torqueable Microcatheters for Coating Defects
Boston Scientific is recalling 381 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/J/1RO/155; Material Number: M001195280
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0193-2027·2026-10-28
B Braun SAFSITE Injection Site Valve Recall for Leakage Risk
B Braun Medical Inc is recalling SAFSITE Injection Site valves due to a potential for leakage and backflow.
Product
B Braun SAFSITE Injection Site, RV1000NC SAFSITE VALVE W/O EXTRA CAP. Catalog Number: 415068.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0242-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 76 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/027/BERN/1RO/105; Material Number: M001195430
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0199-2027·2026-10-28
Philips Smart-hopping 2.0 AP Recall for Wireless Roaming Issues
Philips North America is recalling 174 Smart-hopping 2.0 AP units due to unreliable wireless roaming behavior that can cause loss of connectivity to the central monitoring system.
Product
Philips Smart-hopping 2.0 AP 1.4 GHz; Product/Model Number: 867216;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0237-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 748 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/BERN/2RO/130; Material Number: M001195340
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0246-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 45 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/027/J/1RO/155; Material Number: M001195480
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0236-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 206 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/STRAIGHT/2RO/155; Material Number: M001195330
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0195-2027·2026-10-28
Medtronic NDI Passive Spheres Recalled for Reflective Material Variation
Medtronic is recalling NDI Passive Spheres because variation in the reflective material may affect the navigation system's ability to detect and track the spheres.
Product
Medtronic NDI Passive Spheres REF: 8801074, Sterile EO, 4/Tray 12 Pk., Rxonly
Category
Medical Device
Distribution
52 states
ModerateFDA (Drugs)·D-0059-2027·2026-10-28
Pritam International Recalls evo Fluoride Toothpaste for CGMP Deviations
Pritam International is voluntarily recalling 405,336 tubes of evo toothpaste nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Product
evo, Advanced Whitening, Anticavity Fluoride Toothpaste, (sodium fluoride 0.24%) Peppermint, Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-886-19, Item# 88619, UPC 8 10147 88619 7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0055-2027·2026-10-28
Pritam International Recalls Brush Buddies Toothpaste Due to CGMP Deviations
Pritam International is voluntarily recalling 320,232 tubes of Brush Buddies toothpaste nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Brush Buddies, Crayola, Silly Scents, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Bubble Gum Flavor, Net Wt. 4.0 oz (113g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-003-40, Item # 32731, UPC 8 50048 32731 3
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0256-2027·2026-10-28
Boston Scientific Recalls Direxion Torqueable Microcatheters Due to Defects
Boston Scientific is recalling 378 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/FATHOM/027/STRAIGHT/1RO/155; Material Number: M001195720
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0064-2027·2026-10-28
Brush Buddies Toothpaste Recalled for CGMP Deviations
Pritam International is voluntarily recalling Brush Buddies toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Brush Buddies, Chocolate Ice Cream Flavored Toothpaste, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-518-35, Item # 88518, UPC 8 10147 88518 3
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0279-2027·2026-10-28
Medline Tubal Ligation Kits Recalled for Adhesive Removal Issues
Medline Industries is recalling three tubal ligation kits because they are difficult to remove from patients and leave adhesive residue on the skin.
Product
MEDLINE medical convenience kits labeled as: TUBAL LIGATION RFD, Medline Product Number/SKU DYNJ906291G
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0197-2027·2026-10-28
Medtronic Biopsy Needle Kit Recalled for Reflective Material Variation
Medtronic is recalling 3,746 Biopsy Needle Kits because variation in the reflective material may affect the navigation system's ability to detect and track the spheres.
Product
Medtronic Biopsy Needle Kit, REF: 9733068, Passive, Sterile EO, Rxonly
Category
Medical Device
Distribution
52 states
ModerateFDA (Devices)·Z-0247-2027·2026-10-28
Boston Scientific Recalls Direxion Torqueable Microcatheters for Coating Defects
Boston Scientific is recalling 1,349 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/027/SWAN/1RO/130; Material Number: M001195500
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0230-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 1,912 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/J/1RO/130; Material Number: M001195270
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0062-2027·2026-10-28
Pritam International Recalls Brush Buddies Toothpaste Due to CGMP Deviations
Pritam International is voluntarily recalling 112,092 tubes of Brush Buddies Mint Chocolate Chip Ice Cream Flavored Toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Brush Buddies, Mint Chocolate Chip Ice Cream Flavored Toothpaste, Anticavity Fluoride Toothpaste, (sodium fluoride 0.243%) Net Wt. 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-520-35, Item # 88520, UPC 8 10147 88520 6
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0258-2027·2026-10-28
Boston Scientific Recalls Direxion Torqueable Microcatheters Due to Coating Defects
Boston Scientific is recalling 432 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/FATHOM/027/BERN/1RO/155; Material Number: M001195750
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0192-2027·2026-10-28
Think Surgical Square Driver Recalled for Design Specification Failures
Think Surgical is recalling 15 Square Driver units because they failed to meet design specifications, potentially causing pins to stick or wobble during drilling.
Product
Think Surgical Square Driver REF: 109126
Category
Medical Device
Distribution
Distributed nationwide