Alabama recalls
1469 federal recalls on file affecting Alabama - 57 Alabama-specific plus 1412 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-03-25FDA-DeviceHowmedica OsteonicsClass IINationwideStop using Howmedica MICS3 Saw Attachment
A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.
- 2026-03-25FDA-DeviceGEClass IINationwideUpdate GE Centricity Universal Viewer software
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- 2026-03-25FDA-DeviceGEClass IINationwideUpdate GE Centricity Universal Viewer software
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- 2026-03-25FDA-DeviceGEClass IINationwideUpdate GE Centricity Universal Viewer software
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.
- 2026-03-25FDA-DeviceAbbottClass IINationwideStop using Abbott ID NOW flu test kit
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.
- 2026-03-25USDAPublic Health AlertNationwideDo not eat Blackwing Organic Meats beef or pork
Produced Without Benefit of Inspection
- 2026-03-25FDA-FoodSaputoClass IIReturn Great Value cottage cheese to Walmart
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- 2026-03-25FDA-FoodSaputo CheeseClass IIStop using Great Value cottage cheese
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- 2026-03-25FDA-FoodSaputoClass IIStop using Great Value cottage cheese
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- 2026-03-25FDA-FoodSaputoClass IICLOVER SONOMA SOUR CREAM NET WT 8OZ UPC 0 70852 61800 5 & 16OZ UPC 0 70852 61500 4 DISTRIBUTED BY: CLOVER-STORNETTA FARMS LLC PETALUMA, CA 94952
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- 2026-03-25FDA-FoodSaputoClass IIStop using Clover Sonoma cottage cheese
Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.
- 2026-03-25FDA-FoodKradjianClass INationwideStop using MID EAST Jordanian Zaatar spice mix
Undeclared allergen ingredients (sesame and wheat) in Zaatar Spice mix.
- 2026-03-25FDA-FoodWinder LaboratoriesClass IIICheck Winder Laboratories multivitamin bottles
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
- 2026-03-25FDA-DrugApotexClass IINationwideStop using Apotex brimonidine/timolol eye drops
Lack of Assurance of Sterility
- 2026-03-25FDA-DrugSomerset TherapeuticsClass IINationwideStop using Somerset Therapeutics dexamethasone injection
Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs for these impurities: Dexamethasone Sodium Phosphate EP impurity G (Impurity RU 49336) and dexamethasone formate.
- 2026-03-25FDA-DrugStridesClass IINationwideStop using Strides Pharma Children's Ibuprofen
Presence of foreign substance: the firm received complaints for a gel-like mass and black particles in the product.
- 2026-03-25FDA-FoodShaman BotanicalsClass INationwideStop using Shaman Botanicals White Vein tablets
A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.
- 2026-03-24FDA-PRAmneal PharmaceuticalsNationwideStop using Amneal Magnesium Sulfate IV bags
Bridgewater, New Jersey, Amneal Pharmaceuticals LLC is voluntarily recalling one lot of Magnesium Sulfate in Water for Injection, USP, 4g/100mL, IV bag, to the hospital level. A Magnesium Sulfate in Water for Injection pouch was found to contain an IV bag of Tranexamic Acid in 0.7% Sodium Chloride I
- 2026-03-19CPSCYxtdz StoreNationwideStop using Aisstxoer bicycle helmets immediately
The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional stability, and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.
- 2026-03-19CPSCAmazonNationwideStop using Amazon Basics pocket knife
The folding mechanism on the blade can fail to remain properly secured in the closed position, posing a laceration hazard.
- 2026-03-19CPSCElectroluxNationwideStop using oven on recalled Frigidaire ranges
The ovens in the ranges can experience a delayed ignition of the oven's bake burner, posing a risk of burn hazards to users.
- 2026-03-19CPSCGoregentNationwideStop using Goregent infant walkers immediately
The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk of serious injury or death due to a fall hazard.
- 2026-03-19CPSCBUILTNationwideStop using BUILT LUUM light up tumblers
The recalled LED tumblers can break, making the button cell batteries accessible to children and posing choking and ingestion hazards. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 2026-03-19CPSCSpecializedNationwideStop riding Specialized Turbo Como SL bikes
The bike's fork steerer tube can develop a small fatigue crack that can lead to a progressive failure of the fork, posing a fall hazard.
- 2026-03-19CPSCTainoki Fine FurnitureNationwideStop using Tainoki office chairs immediately
The recalled chairs' base can bend, posing a fall hazard.
- 2026-03-19CPSCWagnerNationwideStop using Wagner 900 Series power steamers
The attached hose can get excessively hot and the nozzle/gun can expel hot water during use and after the trigger is engaged, posing a serious burn hazard to consumers.
- 2026-03-18FDA-DeviceMedlineClass IINationwideStop using Medline surgical drapes
Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is used and surgical strikethrough occurs, there may be risk of infection.
- 2026-03-18FDA-DeviceMedlineClass IINationwideStop using Medline Medcrest Surgical Gowns
Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is used and surgical strikethrough occurs, there may be risk of infection.
- 2026-03-18FDA-DeviceMedlineClass IINationwideCheck lot numbers on Medline cardiac drainage kits
The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.
- 2026-03-18FDA-DeviceAltruanClass IINationwideStop using Bisaf Strep A Self-Test
Product not cleared by the FDA.
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