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.

3,272 stored notices name Alabama, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Alabama too — those are in the archive.

Food

Reported Jan 1, 2025

Kirkland Signature ORGANIC EGGS PASTURE-RAISED 24 EGGS, GRADE A LARGE, NET WEIGHT 48OZ (3 LB) 1.36 kg, UPC 0 96619…

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

Handsome Brook Farms, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2025

BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic…

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

Straight Smile, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

LINK MP Reconstruction System Neck Segment (with suture holes, standard, uncemented, L= 35 mm, CCD 126¿, Offset= 31 mm,…

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

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2024

Duravent Silicone Ventilation Tube. Model Number: 240075.

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 25, 2024

Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm…

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

Spectranetics Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 25, 2024

Baker Farms CURLY MUSTARD 16 oz NET WT 16 oz UPC 8 13098 02018 4 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 Dec 18, 2024

BD Pyxis MedStation ES, REF: 323

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 18, 2024

Jarritos Coconut Water 17.5 fl oz cans- 12 cans per carton

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

Tipp Distributors, Inc. dba Novamex

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2024

Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm), CAR-08-US (8mm), CAR-10-US (10mm), CAR-12-US (12mm)

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

Cartiva, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 11, 2024

Organic Hot Agave in the Raw, 10 oz.

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

Cumberland Packing Corp.

FDA (openFDA food enforcement)

Food

Reported Dec 11, 2024

Traditional Country Canning Spaghetti Sauce, Net Wt. 16 oz. (453g), packaged in glass jars with metal lids, 12 jars per…

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

Englewood Cannery

FDA (openFDA food enforcement)

Food

Reported Dec 11, 2024

Jose Madrid Salsa Chipotle Con Queso, Net Wt. 13 oz. (369g), packaged in glass jars; 12 jars per case

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

Michael Zakany LLC

FDA (openFDA food enforcement)

Medical devices

Reported Dec 11, 2024

EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190

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

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 11, 2024

BIORAPTOR Suture Anchors. Tendon/ligament, non-bioabsorbable bone anchor.

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

Smith & Nephew Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

Merlin@home Transmitter REF EX1100 The Merlin@home" (M@h) transmitter is intended to transfer stored data from the…

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

Abbott Medical

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 4, 2024

Curio Spice Co. brand Grains of Paradise (Korerima) - Jar 1.25 oz net wt. UPC: 672975171032

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

Curio Spice Co.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 4, 2024

4.5 x 180 mm REF 28208BKS Aggressive Cutter, sterile, 6x 3.5 x 70 mm REF 28206CBS Full Radius Resector, sterile, 6x 5.5…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

V.A.C. Ulta Therapy Unit REF CAPULTDEV01 & ULTDEV01 The 3M" V.A.C.¿ Ulta Negative Pressure Wound Therapy System is an…

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

Kci USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

RENASYS EDGE The RENASYS¿ EDGE pump is indicated for patients who would benefit from a suction pump (NPWT), as it may…

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

Smith & Nephew Medical, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

Brand Name: Z-800 Infusion System Product Name: Z-800WF Model/Catalog Number: Z-800WF. The Z-800 Infusion system is…

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

Zyno Medical LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoor…

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

Enchroma Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 27, 2024

MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue…

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

Ethicon, Inc.

FDA (openFDA device enforcement)

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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.