State

Alabama product recalls

72,820 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 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

251–275 of 79161

SevereFDA (Food)·H-1280-2026·2026-08-19
Taylor Farms Recalls Marketside Iceberg Salad for Potential Cyclospora Contamination
Taylor Farms is recalling specific Marketside iceberg salad products due to potential Cyclospora contamination. Consumers should check lot codes and discard affected items.
Product
MARKETSIDE ICEBERG SALAD 10/24 oz, UPC 681131328951; MARKETSIDE ICEBERG SALAD 12/12 oz, UPC 681131328944; MARKETSIDE SHREDDED LETT 12/16 oz, UPC 681131532099; MARKETSIDE SHREDDED LETT 12/8 oz, UPC 681131328968; Iceberg only products.
Category
Food
Distribution
27 states
SevereFDA (Drugs)·D-0750-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 9,762 vials of Semaglutide 4.5mg due to the presence of nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-812-03
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2938-2026·2026-08-19
Erbe ERBECRYO 2 Cryosurgical Unit Recalled Due to Rupture Risk
Erbe USA Inc is recalling ERBECRYO 2 Cryosurgical Units because a strong pull on the high-pressure transfer hose may cause the cryoprobe to rupture.
Product
ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2920-2026·2026-08-19
Dermalon Sutures Recalled for Potential Sterile Barrier Packaging Defects
Covidien is recalling Dermalon 4-0 sutures because sterile barrier packaging may be perforated or torn, risking biocontamination and infection.
Product
Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 75CM C14 88861799-31
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1288-2026·2026-08-19
Taylor Farms Recalls Cross Valley Farms Lettuce Due to Cyclospora Risk
Taylor Farms is recalling specific Cross Valley Farms lettuce products due to potential Cyclospora contamination. Consumers should check lot codes and discard or return affected items.
Product
Cross Valley Farms BLEND LETT/ROM 50/50 NOCLR 4/5# Cross Valley Farms BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.
Category
Food
Distribution
27 states
SevereFDA (Food)·H-1291-2026·2026-08-19
Taylor Farms Recalls Garden Salad Mix Due to Potential Cyclospora Contamination
Taylor Farms is recalling specific lots of garden salad mix and lettuce blends due to potential Cyclospora contamination. Consumers should check lot codes and discard affected products.
Product
TAYLOR FARMS BLEND GARDEN SALAD MIX W/ROM 6/5# NATIONAL TAYLOR FARMS BLEND GARDEN SALAD MIX W/ROM 6/5# ND TAYLOR FARMS BLEND LETT/ROM 50/50 NOCLR 4/5# TAYLOR FARMS BLEND LETT/ROM 70/30 NOCOLR 4/5# TAYLOR FARMS BLEND LETT/ROM 80/20 4/5# TAYLOR FARMS LETTUCE SALAD MIX 4/5# Iceberg
Category
Food
Distribution
27 states
SevereFDA (Drugs)·D-0766-2026·2026-08-19
Prestige Recalls Clear Eyes Maximum Itchy Eye Relief Due to Sterility Concerns
Prestige Brands Holdings is recalling Clear Eyes Maximum Itchy Eye Relief eye drops due to a lack of assurance of sterility and potential contamination.
Product
CLEAR EYES MAXIMUM ITCHY EYE RELIEF — CLEAR EYES MAXIMUM ITCHY EYE RELIEF (GLYCERIN AND NAPHAZOLINE HYDROCHLORIDE AND ZINC SULFATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0762-2026·2026-08-19
Shoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations
Shoolin Pharma Chem LLP is recalling Tadalafil USP 1.00 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.
Product
TADALAFIL USP, 1.00 KG, 1KG(1000gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesania, Gujarat, 382715, India, (CAS NO 171596-29-5), NDC 85702-001-08
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0787-2026·2026-08-19
Baxter Recalls Cefazolin Injection Bags Due to Particulate Matter
Baxter Healthcare is recalling 19,032 bags of Cefazolin Injection due to the presence of particulate matter. The affected product is distributed nationwide in the US.
Product
CEFAZOLIN — CEFAZOLIN (CEFAZOLIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0752-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 4,748 vials of Semaglutide 0.9mg due to the presence of nylon and silk particulate matter.
Product
SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0751-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling specific lots of Semaglutide 9mg vials because they contain nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-822-02
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2948-2026·2026-08-19
Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges
Cardinal Health 200, LLC is recalling 52,699 Presource surgical kits because they contain MEDICOM Ritmed Neurological Sponges with unexpected endotoxin variability.
Product
Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK , Catalog Number: PN33NBMYD; 2) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH4; 3) KIT,CHP BASIC NEURO , Catalog Number: PN36NBCH5; 4) KIT, ANT CERVICAL DISC , Catalog Number: PN41
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2933-2026·2026-08-19
OBP Medical Recalls Vaginal Speculums Due to Potential Sharp Edges
OBP Medical is recalling ER-Spec Single-Use Vaginal Speculums because a burr on the plastic blade may create a sharp edge, posing a risk of injury to patients and providers.
Product
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2925-2026·2026-08-19
Medline Bleach Wipes Recalled for Reduced Disinfection Effectiveness
Medline is recalling bleach wipes that may lose potency before expiration, potentially allowing pathogens to survive.
Product
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count, Product Number MSC351450AN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2766-2026·2026-08-19
Baxter Duo-Vent Solution Set Recalled for Air Bubbles in Tubing
Baxter Healthcare is recalling 24,528 units of Duo-Vent Solution Sets due to customer reports of air bubbles in the drip chamber and tubing.
Product
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2923-2026·2026-08-19
Medline Bleach Wipes Recalled for Reduced Disinfection Effectiveness
Medline Industries is recalling Micro-Kill Bleach Germicidal Wipes because reduced bleach concentration may compromise disinfection effectiveness.
Product
Medline Micro-Kill Bleach Germicidal Bleach Wipes,7" x 8", 150 count, 150 count, Product Number MSC351400AN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2945-2026·2026-08-19
Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Product
Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS , Catalog Number: PE13SPAJA; 3) KIT,SINUS , Catalog Number: PE13SPAJB; 4) KIT, SINUS , Catalog Number: PE13SPAJC
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V537000·2026-08-19
E-One Recalls Fire Trucks Due to Hydraulic Valve Defect
E-One is recalling specific 2025-2026 fire trucks because a hydraulic valve defect may prevent outriggers from extending or retracting, potentially delaying emergency response.
Product
E-ONE — E-ONE CYCLONE N, CYCLONE II, TYPHOON N
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2919-2026·2026-08-19
V-Loc 180 Absorbable Wound Closure Device Recalled for Packaging Defects
FDA is recalling V-Loc 180 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that could lead to biocontamination.
Product
V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY PASS FINAL BOX07405V1 BOX BYPASS CARDON BOX01056V2 BOX BYPASS DR LAGAE BOX01482V2 BOX BYPASS KIT DEZEMBER 2025 BOX09222V1 BOX BYPASS KIT NEU BOX 003
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0761-2026·2026-08-19
Shoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations
Shoolin Pharma Chem LLP is recalling Tadalafil USP 0.500 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.
Product
TADALAFIL USP, 0.500 KG, 0.500KG(500gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesania, Gujarat, 382715, India, (CAS NO 171596-29-5), NDC 85702-002-04.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2943-2026·2026-08-19
Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Product
Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK , Catalog Number: SOP30SPBCC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2949-2026·2026-08-19
Cardinal Health Presource Kits Recalled for Endotoxin Variability
Cardinal Health is recalling 616 Presource Kits because they contain sponges with unexpected endotoxin variability.
Product
Cardinal Health Presource Kits: 1) BASIC PACK , Catalog Number: SBA73BPGCA; 2) SPINE PACK , Catalog Number: SNE11SPHKC; 3) SPINE PACK , Catalog Number: SNE11SPHKD; 4) CRANIOTOMY PACK , Catalog Number: S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2936-2026·2026-08-19
BioFire Respiratory Panel 2.1 Recalled for Increased False Negative Results
BioFire Diagnostics is recalling 2,370 pouches of the BIOFIRE Respiratory Panel 2.1 test due to an increase in false negative results.
Product
BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based multiplexed nucleic acid test, in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2918-2026·2026-08-19
V-Loc 90 Absorbable Wound Closure Devices Recalled for Packaging Defects
Covidien, LP is recalling V-Loc 90 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that may cause biocontamination.
Product
V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 GS-25 VLOCM0436 VLOCM0436 VLOCM0003 V-LOC* 90 4-0 CLR 15CM P12X12 VLOCM0003 VLOCM0013 V-LOC* 90 4-0 CLR 30CM P12X12 VLOCM0013 VLOCM0024 V-LOC* 90 3-0 CLR 45CM P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2924-2026·2026-08-19
Medline Bleach Wipes Recalled for Reduced Disinfection Effectiveness
Medline is recalling Micro-Kill Bleach Germicidal Wipes because reduced bleach concentration may compromise disinfection effectiveness, potentially allowing pathogenic microorganisms to survive.
Product
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count, Product Number MSC351410AN
Category
Medical Device
Distribution
Distributed nationwide