State

Tennessee product recalls

73,817 recalls have nationwide distribution and so reach Tennessee. 7,860 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,860
Critical: 1,324
Severe: 1,974
Most recent: 2026-11-04

Of the 7,860 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 1,974 (25%) are Severe.

Which agencies issued them

These figures cover only the 7,860 recalls whose distribution notice names Tennessee specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44276–44300 of 81677

HighFDA (Devices)·Z-0511-2018·2018-02-14
Philips BrightView XCT Gamma Camera Recalled for Collimator Drop Risk
Philips Medical Systems is recalling BrightView XCT gamma cameras because a collimator may drop to the floor during exchange, posing a risk of injury.
Product
BrightView XCT Model 882482 Product Usage: BrightView XCT is a gamma camera for Single Photon Emission Computed Tomography (SPECT) and integrates with an attenuation device consisting of flat panel x-ray imaging components. BrightView XCT produces non-attenuation corrected…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0517-2018·2018-02-14
Panoramic PC-1000 Dental X-ray Units Recalled for Lift Motor Wear
Panoramic Rental Corp. is recalling PC-1000 dental X-ray units because the lift motor may wear if not properly maintained, posing a risk of injury.
Product
PC-1000, PC-1000/Laser1000, Model Numbers 800724-2 & 800724-3
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0507-2018·2018-02-14
Microline ReNew Reusable Grasper and Dissector Tips Recalled for Insulation Failure
Microline Surgical is recalling ReNew Reusable Grasper and Dissector Tips because heat-shrink insulation may split during sterilization, posing a burn risk during surgery.
Product
The ReNew Reusable Grasper and Dissector Tips are to be used with the ReNew Laparoscopic Handpieces and they are indicated for cutting, grasping, dissecting, and coagulation of tissue in endoscopic and laparoscopic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0527-2018·2018-02-14
Angiodynamics Recalls Accu2i Microwave Tissue Ablation Applicators Due to Malfunction
Angiodynamics, Inc. is recalling 14,353 Accu2i pMTA Microwave Tissue Ablation Applicators because coolant ingress may prevent the device from delivering microwave energy.
Product
Accu2i pMTA Applicator, 29 cm LONG, REF/Catalog # 900-601, Model # (UPN) H7879006010, STERILE --- This is only for use with a Sulis V Generator, REF 806-10. Product Usage: The Acculis Accu2i pMTA Microwave Tissue Ablation Applicator is indicated for the intraoperative…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0528-2018·2018-02-14
Angiodynamics Recalls Accu2i Microwave Tissue Ablation Applicators
Angiodynamics, Inc. is recalling Accu2i pMTA Microwave Tissue Ablation Applicators that may fail to deliver energy due to coolant ingress.
Product
Accu2i pMTA Applicator, 19 cm INTERMEDIATE, REF/Catalog # 900-602, Model # (UPN) H7879006020, STERILE --- This is only for use with a Sulis V Generator, REF 806-10. Product Usage: The Acculis Accu2i pMTA Microwave Tissue Ablation Applicator is indicated for the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0509-2018·2018-02-14
Brainlab AIRO Mobile CT System Recalled for Unintended Motion Risk
Brainlab AG is recalling 102 AIRO Mobile CT Systems due to a risk of unintended motion while the system is in transport mode.
Product
AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO is intended to be used for X-ray computed tomography applications for anatomy that can be imaged in the 107cm aperture excluding pediatric patients and patients weighing over 400 lbs. (182 kg).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0516-2018·2018-02-14
Zimmer Biomet Recalls 1.0mm Drill Bits Due to Fracture Risk
Zimmer Biomet is recalling 1,524 non-sterile 1.0mm drill bits because a raw material anomaly may increase the risk of instrument fracture.
Product
DRILL BIT MINI QUICK CONNECT 1.0MM, REF 2312-20-200 & 2312-20-202, NON STERILE
Category
Medical Device
Distribution
35 states
HighFDA (Food)·F-0771-2018·2018-02-14
Chobani Flip Key Lime Crumble Recalled for Gluten Mislabeling
Chobani is recalling Flip Key Lime Crumble yogurt because the packaging incorrectly states 'No Gluten' despite containing wheat.
Product
Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogurt with Graham Crackers & White Chocolate, 4-packs, 4/5.3 oz cups are packaged with a cardboard overwrap. The net wt. of each single serve up is 5.3 oz. and the net wt. of 4-pack is 21.2 oz. The 4-pack overwrap label…
Category
Food
Distribution
41 states
HighNHTSA·18V108000·2018-02-14
Toyota Recalls 2018 Camry V6 Vehicles for Fuel Leak Fire Risk
Toyota is recalling 2018 Camry vehicles with V6 engines because improperly connected fuel pipes may leak fuel, increasing the risk of a fire.
Product
TOYOTA — TOYOTA CAMRY
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0324-2018·2018-02-14
Flawless Beauty Recalls Relumins Advanced Glutathione Kits Nationwide
Flawless Beauty LLC is voluntarily recalling all lots of Relumins Advanced Glutathione kits nationwide because the products were marketed without FDA approval.
Product
Relumins Advanced Glutathione kits, 900 mg vials, 1500 mg vials and 3000 mg vials
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0788-2018·2018-02-14
Sister Schubert's Recalls Southern Style Frozen Biscuits for Listeria Risk
Sister Schubert's is recalling Southern Style Frozen Biscuits sold under multiple brands due to a positive Listeria monocytogenes test result.
Product
Southern Style Frozen Biscuits sold under the following brand names: Food Club, Food Lion, Laura Lynn, Lowes Foods, Marshalls, Morning Fresh Farms, Piggly Wiggly, Premium Pick 5, SE Grocers, Shur Fine, Southern Home & Valu Time
Category
Food
Distribution
13 states
HighFDA (Devices)·Z-0514-2018·2018-02-14
Philips Precedence 16 Imaging System Recalled for Collimator Drop Risk
Philips is recalling 1,387 Precedence 16 imaging systems because collimators may drop to the floor during exchange, posing a physical hazard.
Product
Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Griffin) is an imaging system combining the acquisition of single photon nuclear medicine images and images from an x-ray computed tomography system. Precedence may produce non-attenuation corrected and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0525-2018·2018-02-14
ConvaTec Recalls Mislabelled Ostomy Skin Barrier Products
ConvaTec is recalling a portion of Lot 7H02242 SUR-FIT Natura Moldable Durahesive Skin Barrier units that were incorrectly labeled as Natura Moldable Stomahesive Skin Barrier.
Product
SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible Collar, 10 pack, 45 mm, REF 411802. Intended for use as an ostomy protector providing a protective barrier to patient skin.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0548-2018·2018-02-14
Zimmer Biomet Recalls Humeral Guide Wires Due to Packaging Design Verification Gap
Zimmer Biomet is recalling 1,517 units of M/DN Intramedullary Fixation Humeral Guide Wires because the previous packaging configuration lacked design verification for 70cm lengths.
Product
M/DN Intramedullary Fixation Humeral Guide Wire - Bullet Tip 2.4 mm Diameter 70 cm Length Single Use Only, Item Number 00-2255-026-00 Product Usage: The Ball Tip and Tear Drop Guide Wires are used during the initial reaming of the intramedullary canal. They also assists in…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0543-2018·2018-02-14
Busse Bone Marrow Biopsy Tray Recalled for Foreign Matter
Robert Busse & Co. is recalling 5 cases of Safety Deluxe Bone Marrow Biopsy/Aspiration Trays due to the presence of loose polypropylene foreign matter.
Product
Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle and Aspiration Needle Sterile, Catalog # 985 Product Usage: Surgical procedure
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0550-2018·2018-02-14
Zimmer Biomet Recalls Natural Nail System Tear Drop Guide Wires
Zimmer Biomet is recalling 10,116 units of Natural Nail System Tear Drop Guide Wires because the previous packaging configuration lacked design verification for 70cm wires.
Product
Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter, 70 cm length, Item Number 47-2490-098-00 Product Usage: The Ball Tip and Tear Drop Guide Wires are used during the initial reaming of the intramedullary canal. They also assists in guiding the nail during…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0338-2018·2018-02-14
McKesson Recalls Subpotent Megestrol Acetate Oral Suspension
McKesson Packaging Services is recalling Megestrol Acetate Oral Suspension because stability testing found the drug was subpotent.
Product
Megestrol Acetate Oral Suspension, USP 400 mg/ 10mL (10 mL UD cups in boxes of 20 cups), Rx Only, Dist. By McKesson Packaging Services a business unit of McKesson Corporation 7101 Weddington Rd. Concord, NC 28027, NDC 63739-549-51
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0548-2018·2018-02-14
Astellas Recalls Mycamine Injection Vials Due to Labeling Error
Astellas Pharma US Inc is recalling 63,600 vials of Mycamine (micafungin sodium) for Injection due to a label error on the declared strength.
Product
MYCAMINE — MYCAMINE (MICAFUNGIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0529-2018·2018-02-14
Angiodynamics Recalls Accu2i pMTA Microwave Tissue Ablation Applicators
Angiodynamics is recalling Accu2i pMTA Microwave Tissue Ablation Applicators because coolant ingress may prevent the device from delivering the desired microwave energy.
Product
Accu2i pMTA Applicator, 14 cm STANDARD, REF/Catalog # 900-600-US, Model # (UPN) H787900600US0, STERILE --- This is only for use with a Sulis V Generator, REF 806-10. Product Usage: The Acculis Accu2i pMTA Microwave Tissue Ablation Applicator is indicated for the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0551-2018·2018-02-14
Zimmer Biomet Recalls Natural Nail System Tear Drop Guide Wires
Zimmer Biomet is recalling 1,631 units of Natural Nail System Tear Drop Guide Wires because the previous packaging configuration lacked design verification for 70cm wires.
Product
Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter, 70 cm length, Item Number 47-2490-098-01 Product Usage: The Ball Tip and Tear Drop Guide Wires are used during the initial reaming of the intramedullary canal. They also assists in guiding the nail during…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0325-2018·2018-02-14
Flawless Beauty Recalls Relumins Vitamin C Ampules for Misbranding
Flawless Beauty LLC is voluntarily recalling all lots of Relumins Vitamin C Solvent ampules because they were marketed without an approved NDA or ANDA.
Product
Relumins Vitamin C Solvent ampules
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0552-2018·2018-02-14
3M Recalls ACE Ultra Lite Ankle Braces Due to Mold Contamination
3M is recalling specific sizes of ACE Ultra Lite Ankle Braces because mold was found on non-patient contact surfaces. The mold was identified as Aspergillus candidus.
Product
ACE(TM) BRAND, ULTRA LITE ANKLE brace: (a) Size Selection Medium, Cat #901014, UPC 051131019984 2; (b) Size Selection Large, Cat #901015, UPC 0 51131019985 9
Category
Medical Device
Distribution
32 states
ModerateFDA (Drugs)·D-0327-2018·2018-02-14
Flawless Beauty Recalls Laroscorbine Platinum Vitamin C Due to Misbranding
Flawless Beauty LLC is voluntarily recalling all lots of Laroscorbine Platinum Vitamin C products because they were marketed without an approved NDA or ANDA.
Product
Laroscorbine Platinum Vitamin C 1 gm Collagen 0.35 gm, Roche
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0542-2018·2018-02-14
Busse Lumbar Puncture Tray Recalled for Foreign Matter
Busse Hospital Disposables is recalling Safety-Deluxe Lumbar Puncture Trays because they may contain loose polypropylene foreign matter above release specifications.
Product
Safety-Deluxe Lumbar Puncture Tray, Catalog # 975 Product Usage: Surgical procedure
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0537-2018·2018-02-14
Medtronic Ascenda Intrathecal Catheter Recall for Kinking Risk
Medtronic is recalling specific lots of Ascenda Intrathecal Catheters due to a potential risk of kinking at the proximal end where the catheter connects to the drug infusion pump.
Product
Medtronic Ascenda(R) Intrathecal Catheter, Models: (a) 8780, UDI: 00643169202122, 00643169783027 (b) 8781, UDI: 00643169202139 (c) 8784, UDI: 00643169202153 The Ascenda Intrathecal Catheter kits (models 8780, 8781 and 8784) contain parts of an infusion system that…
Category
Medical Device
Distribution
Distributed nationwide