Recalls distributed in Alabama
These notices name Alabama in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
3,229 stored notices name Alabama, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Alabama too — those are in the archive.
Reported Feb 22, 2023
iTotal Identity Impactor Handle, Model No. 1080-212/ED-07827 REV AE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Conformis, Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
RipCord Syndesmosis Button, REF: STA001K
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TriMed Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
AxiEM" Non-Invasive Patient Tracker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SynCardia Systems LLC
FDA (openFDA device enforcement)
Reported Feb 3, 2023
FSIS Issues Public Health Alert for Ready-To-Eat Stuffed Chicken Product that May Be Undercooked Due to A Processing…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Vanguard Culinary Group, Ltd.
USDA FSIS
Reported Feb 1, 2023
Getinge Flow-i Anesthesia Systems Flow-i C20, Part no. 6677200 Flow-i C30, Part no. 6677300 Flow-i C40, Part no. 6677400
High riskUsing this product could cause serious injury, illness or death — stop using it now.Getinge USA Sales Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Air-Q3 AirQ3 Standard ILA with Manual Cuff Inflation and GA Size REF Number 0.0 50005 0.5 50055 1.0 50105 1.5 50155 2.0…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SunMed Holdings, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2023
BD Pyxis MedBank System - Product Label/labeling pending
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Dole Chopped Kit BBQ Ranch Green Cabbage, Green Leaf Lettuce, Kale, Carrots, Red Cabbage, Green Onions, Fried Onions,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dole Fresh Vegetables Inc.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2023
Medline CISION Sterile Blades. Labeled as follows with corresponding Item Number. a. STERILE BLADE NO. 10 CARBON STEEL,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
FDA (openFDA device enforcement)
Reported Jan 18, 2023
RadiaLux Lighted Retractor (Pink), REF: 50-101-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2023
Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2023
"Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel states: "Name: Ejiao dates; Ingredients: a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Northern Food I/E Inc.
FDA (openFDA food enforcement)
Reported Jan 4, 2023
Remington MEDICAL, Automatic Cutting Needle, 18ga (1.3mm) x 20cm, REF NAC-1820M (1)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remington Medical, Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2023
XO Marshmallow Limited Edition: Banana Puddin' OMG (Ooey Marshmallow Goodness), 12oz. marshmallow fluff, 4 12oz. retail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.XO Marshmallow, LLC
FDA (openFDA food enforcement)
Reported Dec 28, 2022
X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
DeRoyal MINOR ORAL / ENT PACK, REF 89-2576.15
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
155 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Small Joint OATS Set, REF AR-8981-06S, 6mm; and Small Joint OATS Set, REF AR-8981-08S, 8mm, both containing a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
NextAR Shoulder Surgical Technique, Shoulder NextAR RSA Platform, CT based computer-assisted surgical navigation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medacta USA Inc.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle-USA, Inc. (Corporate Office)
FDA (openFDA food enforcement)
Free recall alerts
Get alerted about new Alabama recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.