Alabama recalls
4377 federal recalls on file affecting Alabama - 369 Alabama-specific plus 4008 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-08FDA-DrugCareFusionClass IINationwideBD ChloraPrep Clear recalled for sterility concerns
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
- 2026-07-08FDA-DrugCareFusionClass IINationwideBD PurPrep applicators recalled for sterility assurance issue
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
- 2026-07-08FDA-DrugCareFusionClass IINationwideBD ChloraPrep Hi-Lite Orange recalled for sterility issue
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel
- 2026-07-08FDA-DrugLupinNot Yet ClassifiedNationwideLupin Glucagon Emergency Kit recalled for plunger defect
CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.
- 2026-07-03FDA-PRPedigreeNationwidePedigree wet dog food recalled for metal and plastic contamination
FRANKLIN, Tenn., (July 2, 2026): Mars Petcare US, Inc. is issuing a voluntary recall for two lots of PEDIGREE® Can High Protein Chopped Chicken & Duck Flavor 13.2oz for dogs.
- 2026-07-03FDA-PRGreenWiseGreenWise frozen blueberries recalled for E. coli O145 risk
July 3, 2026 – Frutas y Hortalizas del Sur S.A., San Carlos, Chile is recalling frozen GreenWise Organic IQF Blueberries 10 oz. Because it may be contaminated with Escherichia coli O145:H28 (E. coli O145).
- 2026-07-02CPSCWinco FireworksNationwideWinco Roman Candles 8 Shot recalled for explosion risk
The recalled fireworks can malfunction, and shots can blow out the side of the tube, posing a risk of serious injury from explosion and burn hazards.
- 2026-07-02CPSCWinco FireworksNationwideWinco Unity 7 Shot fireworks recalled for explosion risk
The recalled fireworks can tip over, posing a risk of serious injury from explosion and burn hazards.
- 2026-07-02CPSCConairNationwideCuisinart grill brushes recalled for metal bristle ingestion risk
Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.
- 2026-07-02CPSCJSNJ_TechNationwideJunpower CR2032 coin batteries recalled for child poisoning risk
The lithium coin batteries are not sold in child-resistant packaging and do not bear the warning labels as required under Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns and death.
- 2026-07-02CPSCCooper LightingNationwideCooper Lighting high bay LED fixtures recalled for fire risk
The LED's board can overheat or come into contact with the lens or nearby combustible materials, posing a fire hazard.
- 2026-07-02CPSCTargetNationwideTarget Gigglescape popping toy recalled for choking hazard
The clear plastic dome can detach from the blue plastic base, making the small plastic balls inside the toy accessible to children, posing a choking hazard.
- 2026-07-02CPSCPretty-LifeNationwideAMASKY nursing pillows recalled for suffocation risk
The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows?and infant support cushions because they can obstruct an infant's breathing, posing a serious risk of injury or death from suffocation.
- 2026-07-02CPSCRowentaNationwideRowenta X-Force Flex cordless vacuums recalled for battery fire risk
The recalled lithium-ion battery in the vacuum cleaner can overheat and ignite, posing a risk of serious injury from fire and burn hazards.
- 2026-07-02CPSCPOPOOONationwidePOPOOO LED finger lights recalled for battery ingestion risk
The recalled LED finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.
- 2026-07-02CPSCDiamond WipesNationwideCVS Health hemorrhoidal wipes recalled for child poisoning risk
The recalled medicated wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging of the wipes is not child-resistant, posing a risk of serious injury or death from poisoning if the contents of the wipes are ingested by young children.
- 2026-07-02CPSCTopyondNationwideTopyond pool drain ports recalled for entrapment hazard
The recalled drain ports with covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to consumers.
- 2026-07-02CPSCVevorNationwideVevor baby loungers recalled for entrapment and fall risk
The recalled baby loungers violate the mandatory safety standard for?infant sleep products. The sides are too low to contain an infant and the enclosed openings at the foot of the loungers are wider than allowed, posing serious risks of fall and entrapment hazards to infants. In addition, the baby loungers do not have a stand, posing a fall hazard if used on elevated surfaces. These violations create an unsafe sleeping environment and can cause death or serious injury.
- 2026-07-01FDA-PRKaoNationwideOribe Serene Scalp shampoo recalled for bacterial contamination
CINCINNATI--(BUSINESS WIRE)--Kao USA Inc. (“Kao USA”) today issued a voluntary recall of select lots of its Oribe Serene Scalp Densifying Shampoo (8.5 oz and 33.8 oz) in the U.S. and Canada due to the detection of Pluralibacter gergoviae bacteria.
- 2026-07-01FDA-PREunha FisheriesNationwideEunha Fisheries sashimi recalled for undeclared wheat, soy, sesame
July 01, 2026 EUNHA FISHERIES CO., LTD., Busan, Republic of Korea, is recalling certain Sliced Korean Halibut and Flounder Sashimi products because the accompanying soy sauce and vinegar red pepper paste packets contain wheat, soy, and sesame that were not declared in English on the individual condi
- 2026-07-01FDA-DeviceAbiomedClass INationwideAbiomed Impella CP Set recalled for blood clot risk
Potential for thrombus formation during prolonged use of the introducer.
- 2026-07-01FDA-DeviceAbiomedClass INationwideAbiomed Impella CP Set recalled for blood clot risk
Potential for thrombus formation during prolonged use of the introducer.
- 2026-07-01FDA-DeviceAbiomedClass INationwideAbiomed Impella CP introducer recalled for blood clot risk
Potential for thrombus formation during prolonged use of the introducer.
- 2026-07-01FDA-DeviceAbiomedClass INationwideAbiomed Impella CP Introducer Kit recalled for blood clot risk
Potential for thrombus formation during prolonged use of the introducer.
- 2026-07-01FDA-DeviceMedlineClass IINationwideMedline surgical kits recalled for unapproved design changes
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- 2026-07-01FDA-DeviceMedlineClass IINationwideConvenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. PICC LINEPACK (PCLUI)642-LF DYNJ47717A
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- 2026-07-01FDA-DeviceMedlineClass IINationwideMedline syringe kits recalled for unapproved design changes
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- 2026-07-01FDA-DeviceMedlineClass IINationwideMedline syringe kits recalled for unapproved design changes
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- 2026-07-01FDA-DeviceMedlineClass IINationwideMedline medical kits recalled for unapproved syringe design changes
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
- 2026-07-01FDA-DeviceMedlineClass IINationwideConvenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO PACK DYNJ30565C DYNJ32555B ANGIO PACK-LF DYNJ0774765U ANGIO TRAY DYNJ46153A ANGIOGRAM TRAY DYNJ33638K ANGIOGRAPHY DRAPE PK QVH-LF DYNJ35110D ANGIOGRAPHY PACK DYNJ44293D ANGIOGRAPHY PACK-LF DYNJ0854485T DYNJ35916J GENERAL ANGIO PACK DYNJ57760B GENERAL ENDO PACK-LF DYNJ0842873J JUDKINS PACK DYNJ51126A RADIOLOGY ANGIO MAJOR PACK DYNJ62
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.
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