State

Tennessee product recalls

73,716 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 73,716 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51–75 of 81575

ModerateFDA (Drugs)·D-0061-2027·2026-10-28
Brush Buddies Toothpaste Recalled for CGMP Deviations
Pritam International is voluntarily recalling Brush Buddies toothpaste nationwide due to CGMP deviations. No illnesses or injuries are reported.
Product
Brush Buddies, Vanilla 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 84140-517-35, Item # 88517, UPC 8 10147 88517 6
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0069-2027·2026-10-28
Pritam International Recalls ARU Toothpaste Due to Manufacturing Deviations
Pritam International is voluntarily recalling 15,264 tubes of ARU Toothpaste due to Current Good Manufacturing Practice (CGMP) deviations. The product was distributed nationwide in the US.
Product
ARU, Toothpaste, Cavity Protection, 9 Ingredients, Cool Mint, (sodium fluoride 0.243%) Net Wt 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-785-35, Item # 88785, UPC 8 10147 88785
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0045-2027·2026-10-28
Ascend Recalls Amlodipine and Olmesartan Medoxomil Tablets for Dissolution Issues
Ascend Laboratories is recalling 11,424 bottles of Amlodipine and Olmesartan Medoxomil tablets because they failed to meet dissolution specifications.
Product
AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0224-2027·2026-10-28
Boston Scientific Recalls Direxion Torqueable Microcatheters for Coating Defects
Boston Scientific is recalling 2,547 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/1RO/130; Material Number: M001195210
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0268-2027·2026-10-28
Solstice Xact Mole Markers Recalled for Detaching Radiopaque Material
Solstice Corporation is recalling 736 Xact mole markers for mammography because the radiopaque material may detach, causing imaging artifacts.
Product
Xact mole marker for mammography Model/Catalog Number: M15RM
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0241-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific Cork, Ltd. is recalling 228 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/STRAIGHT/1RO/155; Material Number: M001195420
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0238-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 384 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/155; Material Number: M001195350
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0063-2027·2026-10-28
Pritam International Recalls Brush Buddies Toothpaste Due to CGMP Deviations
Pritam International is voluntarily recalling 112,092 tubes of Brush Buddies toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Brush Buddies, Cookies 'n Cream 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 84140-519-35, Item # 88519, UPC 8 10147 88519 0
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0251-2027·2026-10-28
Boston Scientific Recalls Direxion Torqueable Microcatheters Due to Coating Defects
Boston Scientific is recalling 3,145 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/FATHOM/021/BERN/1RO/130; Material Number: M001195640
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0191-2027·2026-10-28
Abbott Recalls Amplatzer Amulet Left Atrial Appendage Occluder Devices
Abbott is recalling Amplatzer Amulet Left Atrial Appendage Occluder devices to update instructions for use regarding the risk of pulmonary artery injury.
Product
Amplatzer Amulet Left Atrial Appendage Occluder Model Numbers 1. 9-ACP2-007-016 2. 9-ACP2-007-018 3. 9-ACP2-007-020 4. 9-ACP2-007-022 5. 9-ACP2-010-025 6. 9-ACP2-010-028 7. 9-ACP2-010-031 8. 9-ACP2-010-034
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0264-2027·2026-10-28
restor3d MTP Implant Recall Due to Sterilization Indicator Failure
restor3d Inc. is recalling 16 restor3d MTP Implants because field findings showed orange sterilization indicators, meaning the devices were not exposed to sterilization.
Product
Generic Name: restor3d MTP Implant Generic Name: MTP Implant Model/Catalog Number: 1103-161620 Software Version: None Product Description: The restor3d Metatarsophalangeal (MTP) Implant is a sterile, single-use implant grade metal device, available in varied articulating…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0253-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 156 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/021/STRAIGHT/2RO/130; Material Number: M001195660
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0243-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 620 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/130; Material Number: M001195440
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0275-2027·2026-10-28
Medline Medical Convenience Kits Recalled for Adhesive Removal Issues
Medline Industries is recalling 26,965 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 (list truncated)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0204-2027·2026-10-28
CooperVision recalls Softmed Breathables Advanced Toric contact lenses for labeling error
CooperVision is recalling Softmed Breathables Advanced Toric contact lenses because the packaging incorrectly states they are for extended wear, though they are only approved for daily wear.
Product
Generic Name: Softmed Breathables Advanced Toric (fanfilcon A) Soft (Hydrophilic) Contact Lens; Model/Catalog Number: Softmed Breathables Advanced Toric Product Description: 55% water content, toric, silicone hydrogel contact lens for daily wear, frequent replacement. Blister…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0263-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 550 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Product
Direxion Torqueable Microcatheter, NGMC/TRANSEND/027/BERN/1RO/130; Material Number: M001195940
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0068-2027·2026-10-28
ARU Toothpaste Recalled for CGMP Deviations
Pritam International is voluntarily recalling 15,264 tubes of ARU Toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
Product
ARU, Toothpaste, Gum Health, 9 Ingredients, Soothing Mint, (stannous fluoride 0.45%) Net Wt 3.5 oz (99g), Distributed by Ashtel Studios Inc., Ontario, California 91761, NDC 84140-786-35, Item # 88786 UPC 8 10147 88786 6
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0229-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 358 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/105; Material Number: M001195260
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0278-2027·2026-10-28
Medline recalls medical convenience kits due to removal difficulty and skin residue
Medline Industries is recalling 146,971 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: (list truncated)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0235-2027·2026-10-28
Boston Scientific Recalls Defective Direxion Torqueable Microcatheters
Boston Scientific is recalling 632 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/130; Material Number: M001195320
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0281-2027·2026-10-28
Medline Recalls Hip Scope Packs Due to Removal Difficulties
Medline Industries is recalling 56 hip scope packs because they are difficult to remove and leave adhesive residue on patient skin.
Product
MEDLINE medical convenience kits labeled as: 1) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64103C; 2) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64155B.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0076-2027·2026-10-28
Hikma Recalls Abirtega Tablets for Weight Uniformity Failures
Hikma Pharmaceuticals is recalling Abirtega (abiraterone acetate) 250 mg tablets because they failed weight uniformity specifications.
Product
ABIRTEGA — ABIRTEGA (ABIRATERONE ACETATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0271-2027·2026-10-28
Medline C-Section Drapes Recalled for Adhesive Removal Issues
Medline Industries is recalling C-section drapes that are difficult to remove and leave adhesive residue on patient skin.
Product
MEDLINE DRAPE C-SECTION FEN CLR SCREEN W, Medline Product Number/SKU DYNJP6108
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0240-2027·2026-10-28
Boston Scientific Recalls Direxion Torqueable Microcatheters for Coating Defects
Boston Scientific is recalling 902 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/STRAIGHT/1RO/130; Material Number: M001195410
Category
Medical Device
Distribution
Distributed nationwide
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