State

Tennessee product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33176–33200 of 81600

HighFDA (Drugs)·D-0834-2020·2020-02-19
Zydus Recalls Ethacrynate Sodium Injection Vials Due to cGMP Deviations
Zydus Pharmaceuticals is recalling 2,207 vials of Ethacrynate Sodium for Injection due to current Good Manufacturing Practice (cGMP) deviations.
Product
Ethacrynate Sodium for Injection, USP, 50mg/vial, Single Dose Vial, Rx Only, Manufactured by: Cadila Healthcare Limited, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-246-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1182-2020·2020-02-19
Arrow International Recalls FlexTip Plus Epidural Catheterization Kits
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Product
FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05503-BID
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1187-2020·2020-02-19
Arrow International Recalls Epidural Catheterization Kits Due to Syringe Failures
Arrow International is recalling 343,105 epidural catheterization kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Product
EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LIN
Category
Medical Device
Distribution
37 states
HighNHTSA·20V094000·2020-02-19
BMW Recalls 2014-2019 M6 Gran Coupe for Loose Third Brake Light
BMW is recalling 2014-2019 M6 Gran Coupe vehicles because the third brake light may detach, creating a road hazard and reducing visibility for following traffic.
Product
BMW — BMW M6
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1145-2020·2020-02-19
Philips VesselNavigator Software Recall for DSA Display Defect
Philips is recalling VesselNavigator software due to a defect that displays digital subtraction angiography images without subtraction.
Product
VesselNavigator application used with Philips Azurion (Azurion 7 Series) Software R1.2 and R2.0, and Philips Allura Xper R9, upgraded to Azurion 1.2 M20. System codes: Azurion 7 B12 (722067), Azurion 3 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079), Field…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1152-2020·2020-02-19
Respironics V60 Ventilator Recalled for Frozen Touchscreen Failure
Respironics is recalling 2,851 V60 Ventilators because the touchscreen may freeze, preventing clinicians from adjusting therapy settings. This could delay necessary changes, potentially leading to hypercarbia or hypoxemia.
Product
Respironics V60 Ventilator, Service # 850008, REF: 1053613, 1053614, 1053617, 1053614
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1189-2020·2020-02-19
Arrow International Recalls Epidural Catheterization Kits Due to Syringe Failure Risk
Arrow International is recalling 343,105 epidural catheterization kits because the included syringes may fail, potentially causing dural puncture.
Product
EPIDURAL CATHETERIZATION KIT, Product Code BE-05400-DCHH
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1109-2020·2020-02-19
Terumo Advanced Perfusion System 1 Roller Pump Recall for Shaft Failure
Terumo is recalling 106 Advanced Perfusion System 1 Roller Pumps because the pump shafts may fail, potentially causing the pump to stop during surgery.
Product
Terumo Advanced Perfusion System 1 Roller Pump, 6 Inch, Catalog Number 816571 - Product Usage: is indicated for use for up to 6 hours in the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V095000·2020-02-19
BMW Recalls 2020 X6 Models Due to Rear Spoiler Detachment Risk
BMW is recalling 2020 X6 vehicles because the rear spoiler may detach while driving, creating a road hazard and increasing the risk of a crash.
Product
BMW — BMW X6
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1202-2020·2020-02-19
Arrow International Recalls FlexTip Plus Epidural Catheterization Sets
Arrow International is recalling FlexTip Plus Epidural Catheterization Sets because the included syringes may fail, potentially causing dural puncture.
Product
FlexTip Plus Epidural Catheterization Set, Product Code JC-05400-DCS
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1204-2020·2020-02-19
Arrow International Recalls Epidural Catheterization Kits Due to Syringe Failures
Arrow International is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Product
EPIDURAL CATHETERIZATION KIT, Product Code JC-05400-LB
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1124-2020·2020-02-19
Flowonix Prometra Implantable Pump Recall for Firmware Alarm Anomaly
Flowonix Medical Inc is recalling Prometra Programmable 20mL implantable infusion pumps due to a firmware defect that may prevent the device from sending error codes or audible alarms during valve system issues.
Product
Prometra Programmable 20mL Pump. Catalog No. 91827 The device is an implantable infusion pump. GTIN-14 00810335020XXX (XXX = in-country language specific)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1150-2020·2020-02-19
Medtech ROSA Brain 3.0 Software Recalled for Image Reconstruction Errors
Medtech SAS is recalling ROSA Brain 3.0 software because cross-sectional images may not display properly, potentially compromising surgery planning.
Product
ROSA Brain 3.0 Application-Brain
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1154-2020·2020-02-19
Respironics Ventilator Touchscreen Recall Due to Unresponsive Controls
Respironics is recalling V60/V680 ventilator touchscreens that may freeze and fail to respond to touch commands, potentially delaying necessary therapy adjustments.
Product
Respironics RP-Touch Screen, V60/V680 Ventilator Serviced with Touchscreen RP Kit 453561511951 containing a touchscreen labeled as raw part number 1132318 Revision C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1107-2020·2020-02-19
bioMerieux Recalls VIDAS Varicella Zoster IgG Antibody Test Kits
bioMerieux is recalling VIDAS Varicella Zoster IgG antibody kits due to potential invalid calibrations or false positive results.
Product
VIDAS Varicella Zoster IgG (VZG) antibody IVD, kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1155-2020·2020-02-19
Respironics V680 Ventilator Recalled for Unresponsive Touchscreen
Respironics is recalling 190 V680 Ventilators because the touchscreen may freeze, preventing clinicians from adjusting therapy settings and potentially causing delayed treatment.
Product
Respironics V680 Ventilator, Service # 850011, (OUS Only)
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20074·2020-02-19
Contigo Recalls 5.7 Million Kids Water Bottles Due to Choking Hazard
Contigo is reannouncing a recall of 5.7 million kids water bottles because the clear silicone spout can detach, posing a choking hazard to children.
Product
Contigo Kids Cleanable Water Bottles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1217-2020·2020-02-19
Arrow International Recalls FlexTip Plus Epidural Catheterization Kits
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Product
FlexTip Plus Epidural Catheterization Kit, Product Code YC-02220
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1207-2020·2020-02-19
Arrow International Recalls FlexTip Plus Epidural Catheterization Kits
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits due to potential syringe failures that could cause dural puncture.
Product
FlexTip Plus Epidural Catheterization Kit, Product Code MP-17019-TKP
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1121-2020·2020-02-19
Flowonix Prometra II Pump Recall for Firmware Alarm Anomaly
Flowonix Medical Inc is recalling Prometra II 20mL implantable infusion pumps due to a firmware defect that may prevent the device from sending error codes or audible alarms for valve system issues.
Product
Prometra II 20mL Pump. Catalog No. 13827 The device is an implantable infusion pump. GTIN-14 00810335020228
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1110-2020·2020-02-19
Terumo Advanced Perfusion Assembly Pump Guts Recalled for Potential Shaft Failure
Terumo is recalling 16 Advanced Perfusion Assembly Pump Guts units because the pump shafts may fail, potentially causing the pump to stop during surgery.
Product
Terumo Advanced Perfusion Assembly Pump Guts, 6 Inch, Catalog Number 801798 - is indicated for use for up to 6 hours in the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a qualified medical…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1123-2020·2020-02-19
Flowonix US Clinical 20mL Programmable Pump Recall for Firmware Alarm Defect
Flowonix Medical Inc is recalling US Clinical 20mL Programmable Pumps because a firmware anomaly may prevent the device from sending error codes or audible alarms during valve system issues.
Product
US Clinical 20mL Programmable Pump. Catalog No. 01827 The device is an implantable infusion pump. GTIN-14 00810335020082
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1125-2020·2020-02-19
Flowonix Prometra II Pump Recall for Firmware Alarm Anomaly
Flowonix Medical Inc is recalling Prometra II implantable infusion pumps because a firmware anomaly may prevent the device from sending error codes or audible alarms.
Product
Prometra II Programmable 20mL Pump. Catalog No. 93827 The device is an implantable infusion pump. GTIN-14 00810335020YYY (YYY= in-country language specific)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0841-2020·2020-02-19
Pfizer Recalls Caduet Tablets Due to Defective Bottle Seals
Pfizer is recalling 141 bottles of Caduet tablets because defective bottle rims may have allowed moisture to enter, potentially compromising the medication.
Product
CADUET — CADUET (AMLODIPINE AND ATORVASTATIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0837-2020·2020-02-19
Teva Recalls Methylphenidate Hydrochloride Extended-Release Tablets Due to Missing Desiccant
Teva Pharmaceuticals USA is recalling 17,436 bottles of Methylphenidate Hydrochloride Extended-Release tablets because the product bottles may be missing desiccant.
Product
METHYLPHENIDATE HYDROCHLORIDE — METHYLPHENIDATE HYDROCHLORIDE (METHYLPHENIDATE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide