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.
Reported Jul 9, 2025
Change Healthcare Cardiology Hemo Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Change Healthcare Canada Company
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2025
Family Garden Salad - 24 oz 63912388065 Garden Salad - 12 oz 63912388067 Family Cobb Salad - 22 oz 63912388068 Cobb…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jfe Franchising Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 9, 2025
Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans sold as an individual flavor and in variety packs of 12, 24,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Peak Cocktails
FDA (openFDA food enforcement)
Reported Jul 2, 2025
REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2025
REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 2, 2025
Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen Cap LCAP Firmware 1.3.0 Release…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bigfoot Biomedical
FDA (openFDA device enforcement)
Reported Jul 2, 2025
Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2025
Carley s Soft Baked Iced Lemon Cookies, 5.34oz Plastic Tray, clear film overwrap w/ Label, 12 units per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carley's Inc.
FDA (openFDA food enforcement)
Reported Jun 25, 2025
CPK TEQUILA LIME BASE ALLERGENS: MILK NET WEIGHT: 1 LB Case UPC FG15453558 Manufactured for California Pizza Kitchen,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bakkavor Foods USA, Inc.
FDA (openFDA food enforcement)
Reported Jun 25, 2025
Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Balt USA, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Covidien
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Microtek Patient Drape ECOLAB AP6MMN Patient Drape, 6mm Adapter Plug Kit REF AP6MMN UDI code: (01)10748426139986 AP8MMN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microtek Medical, Inc.
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse Blood, REF CP11410;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel, Inc.
FDA (openFDA device enforcement)
Reported Jun 18, 2025
Long Nail, RIGHT Gamma4 10x320mm x 125, component of the Gamma4 System. Catalog Number: 84250320S.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 11, 2025
Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Mishima K.K.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 11, 2025
GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.GNC Holdings LLC
FDA (openFDA food enforcement)
Reported Jun 11, 2025
VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test, REF 20-006-021; for use with the sample-to-results…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Jun 11, 2025
Greenwise Pear Kiwi Spinach & Pea Baby Food Pouch. Net Wt 4 oz. (113g). Stage 2 6 months+, Best if" date of 11/01/2025.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Publix Super Markets, Inc.
FDA (openFDA food enforcement)
Reported Jun 4, 2025
Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5 and 5 French UVCs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 4, 2025
ABBOTT RAPID DX N AMERICA LLC MULTI ANALYTE LVL1&2250UL CHOLS CONTROL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical-Surgical Inc. Corporate Office
31 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 4, 2025
Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number: 10995498
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 May 28, 2025
BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN, REF: 386865; BD Cathena Safety IV Catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems, Inc.
FDA (openFDA device enforcement)
Reported May 28, 2025
Bard Minnesota Four Lumen Esophagogastric Tamponade Tube, REF:0092220 18 Fr. (6mm, 7/32"), 41" Length (104cm) with 8"…
High riskUsing this product could cause serious injury, illness or death — stop using it now.C.R. Bard Inc.
4 more products in this recall
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.