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 Aug 3, 2022
REF: 4P52-20 Hemoglobin A1c for use with Architect, IVD, CE, R1 1 x 52 mL, R2 1 x 20 mL, A1cDL 2 x 35 mL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Da Vinci S/Si Large Clip Applier, Model 420230 Da Vinci S/Si Medium-Large Clip Applier, Model 420327 Da Vinci S/Si…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Sight OLO, Automated Hematology Analyzer, Catalog No. OLO-U1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sight Diagnostics Ltd.
FDA (openFDA device enforcement)
Reported Jul 27, 2022
ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with EnduRo Total Knee System. instrument used during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Item 38180-12, Chuckanut Bay Cheesecake Bites New York + Chocolate. Perishable - Keep Refrigerated. There are 8 pieces…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chuckanut Bay Foods LLC
14 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2022
LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2022
Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jul 27, 2022
NeuRx Diaphragm Pacing System (NeuRx DPS), Affected part numbers: Part # Part Name 20-0035 NeuRx DPS System Kit 20-0036…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Synapse Biomedical Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Morphine Sulfate extended-Release Tablets, USP; 30 mg, 100-count bottles, Rx only, manufactured by: Ohm Laboratories…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bryant Ranch Prepack, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 20, 2022
PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System, Catalog numbers PG2990BPS, PG2990BPX,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis US Corp.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Isopure Sodium Bicarbonate Mixing and Distribution System (IsoMix PRO)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Isopure Corp.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Favorite Day Lavender Shortbread Cookie Bites Net Wt 7oz (198g) packaged in a purple bag and an inside silver flexible…
High riskUsing this product could cause serious injury, illness or death — stop using it now.J & M Foods, Inc.
FDA (openFDA food enforcement)
Reported Jul 20, 2022
MiniMed 620G Insulin Pump (O.U.S. version)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2022
epoc BGEM Test Card 25 Test Cards/box. In vitro diagnostic device for the quantitative testing of samples of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Ventana HE 600 System, automated slide preparer, for use in laboratories.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2022
Endo Model Modular Rotational Tibia - Small (Model No #15-2814/02), Medium (Model No #15-2814/03), and Large (Model No…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Mfg Site)
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2022
CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zeltiq Aesthetics, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
Palindrome Precision Chronic Catheter, Sterile, Single Use, Rx Only. For vascular access for acute and chronic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2022
Dimension LTNI -In vitro diagnostic test intended to quantitively measure cardiac troponin-I levels in human serum and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 6, 2022
DVR Anatomic, Model No. DVRAR. Distal Volar Radius Anatomical Plate System used for the fixation of fractures and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Changzhou Biomet Medical Devices Co., Ltd.
FDA (openFDA device enforcement)
Reported Jul 6, 2022
QMS Tacrolimus Immunoassay REF 10015573 CALIBRATOR SET QMS TACROLIMUS CAL A 10015566-3 QMS TACROLIMUS CAL B 10015567-3…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
FDA (openFDA device enforcement)
Reported Jul 6, 2022
Snack Fresh Apples and Peanut Butter Net Wt 6.5 oz. packed in clear plastic non-flexible package UPC 0 74641 00044 6…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stellex/CF Houston, LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 6, 2022
Volcano Visions PV. 035 Digital IVUS Catheter REF 88901, PN: 300005384002 Rx Only, Sterile EO, CE 2797
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Volcano Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 29, 2022
Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Peach Mango Natural & Artificial Flavor, 33.8 FL OZ (1.05…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
1 more product in this recall
FDA (openFDA food 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.