State

Alabama product recalls

72,984 recalls have nationwide distribution and so reach Alabama. 6,341 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,341
Critical: 1,121
Severe: 1,337
Most recent: 2026-09-02

Of the 6,341 recalls naming Alabama we have scored against our rubric, 1,121 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,337 (21%) are Severe.

Which agencies issued them

These figures cover only the 6,341 recalls whose distribution notice names Alabama specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6251–6275 of 79325

SevereFDA (Drugs)·D-0499-2025·2025-07-09
Bupivacaine HCL Sterile Injection Recalled for Sterility Assurance Concerns
Tailstorm Health Inc. is recalling bupivacaine HCL sterile injection vials nationwide due to FDA inspection findings regarding concerns with the sterile manufacturing process.
Product
BUPIVAcaine HCL Sterile injection, USP w/EPINEPHRINE 1:200,000, 50 mg/10mL, 0.5%, (5mg/mL), 10 mL Sterile Single-Dose Vial, Rx Only, For Nerve Block, Caudal & Epidural Anesthesia Only, Warning: Contains Sulfites, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2035-2025·2025-07-09
BiPAP V30 Auto ventilators are not indicated for respiratory failure
The Philips Respironics BiPAP V30 Auto Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 5,958 units affected.
Product
BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory support for pediatric and adult patients weighing over 10 kg.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0505-2025·2025-07-09
Zicam Nasal AllClear swabs recalled over fungal contamination of swabs
Zicam Nasal AllClear swabs are being recalled because of fungal contamination of the nasal swabs. All lots are affected, covering 13,632 cartons.
Product
ZICAM NASAL ALLCLEAR, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc.., Ewing NJ. UPC 7 32216 30165 6
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0506-2025·2025-07-09
Orajel Baby teething swabs recalled over fungal contamination of swabs
Orajel Baby Cooling Swabs for Teething are being recalled because of fungal contamination of the infant oral swabs. All lots are affected, covering 695,880 cartons.
Product
Orajel Baby, Cooling Swabs for Teething, Each Unit 0.007 fl oz (0.22 mL), NET 0.08 FL OZ (2.6 mL) TOTAL, 12 Single-Use Swabs per carton, Manufactured for Church & Dwight Co. Inc. Ewing. NJ 08328 USA. UPC CODE 3 10310 40000 2.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2037-2025·2025-07-09
BiPAP A40 ventilators are not indicated for respiratory failure patients
The BiPAP A40 Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 6 units in the US and 67,534 outside it are affected.
Product
BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for the purpose of treating adult and pediatric patients. BiPAP A40 Pro - sold OUS
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2013-2025·2025-07-09
Servo-u ventilators may measure patient circuit compliance inaccurately
The Servo-u Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 874 units are affected.
Product
Servo-u Ventilator System. Model Number: 6688600.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0208-2025·2025-07-09
Bibimbap Bowl recalled due to potential Salmonella contamination
JFE Franchising Inc is recalling 13 oz Bibimbap Bowls (UPC 63912389259) because cucumbers in the product have the potential to be contaminated with Salmonella.
Product
Bibimbap Bowl 13 oz 63912389259
Category
Food
Distribution
7 states
SevereFDA (Drugs)·D-0504-2025·2025-07-09
Zicam cold remedy nasal swabs recalled over fungal contamination
Zicam Cold Remedy Medicated Nasal Swabs are being recalled because of fungal contamination of the swabs. All lots are affected, covering 3,374,918 cartons.
Product
ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0207-2025·2025-07-09
Fruit and Vegetable Trays Recalled for Potential Salmonella Contamination
JFE Franchising Inc. is recalling multiple fruit and vegetable tray products because cucumbers may be contaminated with Salmonella. The affected products were distributed in seven states with a sell-by date of May 20, 2025.
Product
Fruit & Vegetable Tray - 64 oz 63912394047 Mixed Melon, Cucumbers & Tajin - 18oz 63912394007 Watermelon & Cucumber w/ Tajin - 18oz 63912394036 Small Vegetable Tray - 19.5 oz 63912388045 Small Party Tray with Dip - 19 oz 63912388046 Large Vegetable Tray - 42 oz 63912
Category
Food
Distribution
7 states
SevereFDA (Devices)·Z-2015-2025·2025-07-09
Servo-u MR Ventilator System inaccurate patient circuit compliance measurement
Servo-u MR Ventilator System (Model 6888800) may measure patient circuit compliance inaccurately due to incorrect pre-use leakage testing and incorrect active humidifier use.
Product
Servo-u MR Ventilator System. Model Number: 6888800.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0569-2025·2025-07-09
Sandoz cefazolin cartons contained vials labeled as penicillin G potassium
Sandoz Cefazolin for Injection 1 gram is being recalled after cartons were found to contain vials labeled as penicillin G potassium. 208,300 vials are affected.
Product
CEFAZOLIN — CEFAZOLIN (CEFAZOLIN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0205-2025·2025-07-09
Packaged salads recalled because cucumbers may be contaminated with Salmonella
A range of packaged salads is being recalled because the cucumbers used in them have the potential to be contaminated with Salmonella. Affected product carries a sell by date of 5/20/2025.
Product
Family Garden Salad - 24 oz 63912388065 Garden Salad - 12 oz 63912388067 Family Cobb Salad - 22 oz 63912388068 Cobb Salad - 11 oz 63912388069 Cucumber Salad - 3oz 63912389205 Cucumber Salad 3oz 63912389243 Spicy Cucumber Salad 3oz 63912389329 Chef Salad - 11 o
Category
Food
Distribution
7 states
SevereFDA (Food)·H-0209-2025·2025-07-09
Yaki Noodle and Ebi Vermicelli Bowls recalled for Salmonella contamination risk
JFE Franchising Inc. is recalling Yaki Noodle Bowls and Ebi Vermicelli Bowls due to potential Salmonella contamination in cucumbers used in the products.
Product
Yaki Noodle Bowl 12 oz 63912389254 Ebi Vermicelli Bowl 13oz 63912389334
Category
Food
Distribution
7 states
SevereFDA (Food)·H-0206-2025·2025-07-09
Fresh cut cucumber products recalled over potential Salmonella contamination
Fresh cut cucumber products from JFE Franchising, including cucumber with ranch and cucumber with Tajin, are being recalled because the cucumbers may be contaminated with Salmonella.
Product
Cucumber with Ranch - 9 oz 63912395020 Cucumber, Lime & Tajin - 19oz 63912388053 Cucumber Slices w/Tajin - 15 oz 63912388022 Cucumber Bowl w/ Ranch Dressing - 15 oz 63912388063
Category
Food
Distribution
7 states
SevereFDA (Drugs)·D-0503-2025·2025-07-09
Lidocaine HCL Sterile Injection recalled for sterility assurance concerns
Tailstorm Health INC is recalling Lidocaine HCL Sterile Injection (20 mg/mL) due to FDA inspection findings of concerns with the sterile manufacturing process. The recalled product is distributed nationwide.
Product
LIDOcaine HCL Sterile Injection, USP, 20 mg/mL, 2%, (200 mg/10 mL), For Infiltration & Nerve Block, Including Caudal & Epidural Use, Preservative Free, 10mL Sterile Single-Dose Vial, Rx Only, Medivant Healthcare, 158 S. Kyrene Rd., Chandler, AZ, 85226, NDC 81483-0001-0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2014-2025·2025-07-09
Servo-n ventilators may measure patient circuit compliance inaccurately
The Servo-n Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 7,688 units affected.
Product
Servo-n Ventilator System. Model Number: 6694800.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2051-2025·2025-07-09
Philips C9-5EC Ultrasound Transducer Devices Recalled
Philips Ultrasound, Inc. is recalling Philips C9-5EC transducer devices that were refurbished beyond their useful life, which may affect device performance and safety.
Product
Philips C9-5EC Transducer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2072-2025·2025-07-09
Cardiology hemodynamics software update may cause unexpected system shutdowns
Change Healthcare Cardiology Hemodynamics Software version 15.0.1 is being recalled because, following complaints, a software update may cause the software to unexpectedly shut down.
Product
Change Healthcare Cardiology Hemodynamics Software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0501-2025·2025-07-09
Compounded ketamine multi-dose vials recalled over sterility assurance concerns
Ketamine Hydrochloride Injection 500 mg/5 mL multi-dose vials compounded by Medivant Healthcare are being recalled for lack of assurance of sterility. 14,725 vials are affected.
Product
KETAmine Hydrochloride Injection, USP, 500mg/5mL, (10mg/mL), For IM or Slow IV Use, 5mL Sterile Multi-Dose Vial, Rx Only, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene, Rd. Chandler, AZ 85226, NDC 81483-0007-2.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2039-2025·2025-07-09
VITROS XT 7600 Chemistry Analyzer Software Anomaly Causing Erroneous Test Results
Ortho-Clinical Diagnostics is recalling VITROS XT 7600 Integrated System analyzers due to a software anomaly that can report test results as expired when reagent shelf expiration dates are omitted during manual loading, potentially causing erroneous or delayed test results.
Product
Brand Name: VITROS; Product Name: VITROS XT 7600 Integrated System; Model/Catalog Number: (1) 6844461, (2) 6272222; Software Version: version 3.2 to version 3.8.3 (all available software versions); Product Description: In vitro diagnostic chemistry analyzer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2076-2025·2025-07-09
Bard Urologist's Tray Recalled Over Incorrect French Size Labeling
C.R. Bard Inc is recalling 63 units of the Bard Urologist's Tray due to cather packaging that may contain the incorrect French size, which could affect device use.
Product
REF: 123400,Bard Urologist's Tray, For the Obstructed Urethra
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2040-2025·2025-07-09
VITROS 4600 chemistry systems may report results using expired diluent packs
VITROS 4600 Chemistry Systems are being recalled because a software anomaly can allow results to be reported using diluent packs the system treats as expired, which can produce erroneous results.
Product
Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog Number: (1) 6802445, (2) 6900440 Software Version: version 3.2 to version 3.8.3 (all available software versions) Product Description: In vitro diagnostic chemistry analyzer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0502-2025·2025-07-09
Compounded lidocaine with epinephrine vials lack assurance of sterility
Lidocaine HCl Sterile Injection 1% with epinephrine 1:100,000, compounded by Medivant Healthcare, is being recalled for lack of assurance of sterility. 2,825 vials affected.
Product
LIDOcaine HCL Sterile Injection, USP, 100mg/10mL, 1%, (10mg/mL), w/EPINEPHRINE 1:100,000, For Infiltration & Nerve Block, Including Caudal & Epidural Use, 10 mL Sterile Single-Dose Vial, For Office Use Only, Compounded Drug by: Medivant Healthcare, 158 S. Kyrene, Rd. Chandler, AZ
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2074-2025·2025-07-09
BD Heyman Follower Straight Tip catheters with incorrect French size packaging
C.R. Bard Inc is recalling BD Heyman Follower Straight Tip catheters because packaging may contain an incorrect French size designation, which could lead to use of the wrong catheter size.
Product
BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF: 21120
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V450000·2025-07-09
Airstream Recalls 2025-2026 Interstate Motorhomes Due to Awning Lock Failure
Airstream is recalling 2025-2026 Interstate motorhomes because a module may fail to lock controls, allowing the awning to extend during transit and become a road hazard.
Product
AIRSTREAM — AIRSTREAM INTERSTATE
Category
Vehicle
Distribution
Distributed nationwide