Recalls affecting Alabama
Notices that name Alabama in their distribution area, plus every nationwide recall — nationwide recalls reach Alabama too.
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Class II · 4 months ago
Dabur India Limited Med Pride, Bacitracin Zinc Ointment, 500 units, 1oz tubes recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Dabur India Limited Med Pride, Hydrocortisone Cream 1% recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Dabur India Limited Lucky Super Soft, Antifungal Athlete's Foot Cream recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Keystone Industries Quala Dental Products, Topical Anesthetic Gel recall: Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals
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Class II · 4 months ago
Inventia Healthcare Limited Chlorthalidone Tablets, USP, 25 mg recall: Failed Dissolution Specifications
Failed Dissolution Specifications
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Class II · 4 months ago
IntegraDose Compounding Services LLC Vasopressin 2 Units/2 mL in 0.9% Sodium recall: Subpotent Drug
Subpotent Drug
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Class II · 4 months ago
Dabur India Limited Med Pride, Bacitracin Zinc Ointment, 1oz per tube recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Dabur India Limited Lucky Super Soft, First Aid Triple Antibiotic Ointment recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Dabur India Limited Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Dabur India Limited Rapidol, Triple Antibiotic First Aid Ointment recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Keystone Industries PureLife, Topical Anesthetic GEL, Benzocaine 20%, 1 oz recall: Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals
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Class II · 4 months ago
Dabur India Limited Med Pride, Hydrocortisone Cream 1% recall: CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
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Class II · 4 months ago
Keystone Industries DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor recall: Defective container:may contain bottles with incomplete seals
Defective container:may contain bottles with incomplete seals
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Class II · 4 months ago
Nutrisystem, Chocolate Cheesecake, 2 oz packages, Flow Wrapped recall: Undeclared Allergen (Soy)
Undeclared Allergen (Soy)
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Class II · 4 months ago
Fairhope Roasting Company Cold Brew Coffee Concentrate recall: Product requires refrigeration but the label is missing a "Keep Refrigerated"
Product requires refrigeration but the label is missing a "Keep Refrigerated" statement
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Class II · 4 months ago
United States Bakery Great Value Hawaiian Roll 4pk recall: Firm observed oily and sticky substance on direct food contact surface
Firm observed oily and sticky substance on direct food contact surface packaging of finished product.
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Highest risk · 4 months ago
Joolz Aer2 Car Seat Adapters for Strollers recall: Risk of Serious Injury from Fall Hazard
Risk of Serious Injury from Fall Hazard
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Highest risk · 4 months ago
Arizer Solo III portable electronic vaporizers recall: The pajama sets violate the mandatory safety standards for children's
The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.
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Class II · 4 months ago
INSPIREMD Inc CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/ recall: Stent delivery system may encounter complications during deployment
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
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Class II · 4 months ago
Berlin Heart Gmbh EXCOR Pediatric Ventricular Assist Device System recall: Blood pump inner package expiration date does not match the outer-correct
Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.
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Class II · 4 months ago
Abbott Medical Merlin" Patient Care System software Merlin" PCS 3650 programmer Model recall: Software malfunction may occur during pacing capture threshold test
Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command…
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Class II · 4 months ago
GE Medical Systems, LLC Allia IGS 7 Pulse angiographic X-ray system recall: GE HealthCare has become aware of a potential issue affecting an electrical
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue…
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Class II · 4 months ago
Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm recall: The cannulation of the CCS screw is not centered
The cannulation of the CCS screw is not centered.
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Class II · 4 months ago
D.O.R.C. Dutch Opthalmic Research Center Intl B.V. TDC Veloce" recall: An increase in incidence in complaints of a loose outer knife and reports
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.