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 Jan 17, 2024

Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit…

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

Bard Peripheral Vascular Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 17, 2024

Shiloh Farms Bread for Life Organic 7 Grain UPC 0-47593-02812-7

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

Garden Spot Foods, LLC.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 17, 2024

Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS

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

Medtronic Navigation, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2024

Incisive CT, model 728143 & 728144 running Software Version 5.0.0.

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

Philips Healthcare (Suzhou) Co., Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 17, 2024

CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010,…

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

Townsend Design

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

Reverse Shoulder System e+, REF 509-01-032, RSP Humeral Socket Insert, Sz. 32mm, Semi-Constrained, Sterile H2o2, CE 2797

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

Encore Medical, LP

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

Merit Maestro Microcatheter, Reference Numbers: 28MC2111045/B, 28MC21110ST/B, 28MC2113045/B, 28MC21130SN/CNB,…

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

Merit Medical Systems, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

External Drainage System Collection Bag, REF: NT821732C, STERILEEO, Rx only

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

Natus Medical Incorporated

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 10, 2024

Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B…

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

Philips Respironics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 3, 2024

Alinity ci-series System Control Module, REF: 03R70-01

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Jan 3, 2024

RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320, Low Profile Primary Guide is an…

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

Acumed LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 3, 2024

Liberty Select Cycler, Model numbers RTLR180343 and RTLR180111

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

Fresenius Medical Care Holdings, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

Abbott CELL-DYN Ruby, Model CD-Ruby, List number 08H67-01, and Abbott CELL-DYN Sapphire, Model CD Sapphire, list number…

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

Biolox Ceramic Option Head Zimmer 12/14 40mm -3, Item Number 00-8777-040-01

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

Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV…

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

Nurse Assist, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI USA Elite System and USA Series Right Angle Cutting…

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 27, 2023

The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into…

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 27, 2023

AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 27, 2023

Cantaloupe Chunks 9oz (255g) UPC 8 26766 13923 1 & 18 oz (1 LB 2 OZ) 5??g UPC 8 26766 13917 0 Dist By Renaissance Food…

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

Renaissance Food Group

15 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 27, 2023

HMC Farms Peaches 2lb Gusset Bag

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

The HMC Group Marketing Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 20, 2023

Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection

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

Houdini Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 20, 2023

CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP)…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 20, 2023

TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP

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 20, 2023

Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR)…

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

Philips North America LLC

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.