All recall categories

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.

Medical devices

Reported Oct 13, 2021

CardioQuip, Modular Cooler-Heater, Model: MCH-1000(i), CE 2797, UDI: (01)00860000846103

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CardioQuip, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Contamac Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5 LITER/4266, distributed by DJO, LLC / DJO…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Djo, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

ARCH Leg Positioning System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Innovative Orthopedic Technologies, LLC

FDA (openFDA device enforcement)

Food

Reported Oct 13, 2021

KALE NET WT 16 OZ (1 LB) 454g Sold under the following brand names: Baker Farms 3667 Ellenton Norman Park Road, Norman…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Terry and Joe Baker Farms, LLC dba Baker Farms

FDA (openFDA food enforcement)

Medical devices

Reported Oct 13, 2021

Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange Catheter Kit, with central venous infusion…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ZOLL Circulation, Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 6, 2021

DxA 5000 (DxA Automation System, DxA 5000 fit), "For in Vitro Diagnostic Use", Reference Numbers: B87352 with B57634,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 6, 2021

VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Oct 6, 2021

Daytime Severe Cold & Flu Relief 8 Pre-Measured Vials 0.51 FL OZ (15 mL) Each 4.06 FL OZ (120 mL) Total/Nighttime…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

New Vision Pharmaceuticals LLC

1 more product in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 29, 2021

Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

DLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Perfusion Systems

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: EPIQ 5 - 795120 EPIQ 5C - 795205…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

Sight OLO-E1/U1 Software and Operators Manual Software v2.56.1 Catalog #: 1 OLO-U1 Catalog #: 2 OLO-E1 revision 1.9,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sight Diagnostics Ltd.

FDA (openFDA device enforcement)

Food

Reported Sep 29, 2021

Kroger Kale Bag 16oz plastic bag 8 packages per case

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Kroger Co.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 22, 2021

Configura Advance Chair, Model Number: CHAIR-0-SC1-030; Advance Chair, 100mm Castors, Std Backrest, Manual; Serial…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Accora Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carefusion

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

Arjo Disposable Repositioning Sling, Model AHD001

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Getinge Dominican Republic SA

FDA (openFDA device enforcement)

Medical devices

Reported Sep 15, 2021

Pipeline Flex Embolization Device

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Micro Therapeutics Inc.,

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 15, 2021

QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Native Promotions, Inc.

FDA (openFDA drug enforcement)

Food

Reported Sep 8, 2021

Hostess Soft White Hamburger Buns, Net Wt. 12 OZ, UPC 888109110987

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hostess Brands, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 8, 2021

Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Magnolia Medical Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 8, 2021

CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of SARS-CoV-2 Antigen Qualitative detection of the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Versea Diagnostics LLC

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 8, 2021

Cahill Cheddar with Porter PLU 93579 packaged in clear plastic

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Whole Foods Market

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 8, 2021

CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zeltiq Aesthetics, Inc.

FDA (openFDA device enforcement)

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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.