State

Alabama product recalls

72,820 recalls have nationwide distribution and so reach Alabama. 6,341 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,341
Critical: 1,121
Severe: 1,337
Most recent: 2026-09-02

Of the 6,341 recalls naming Alabama we have scored against our rubric, 1,121 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,337 (21%) are Severe.

Which agencies issued them

These figures cover only the 6,341 recalls whose distribution notice names Alabama specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

551–575 of 79161

HighFDA (Devices)·Z-2783-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. PROSTATE ROBOTIC DYNJ901822B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2781-2026·2026-07-29
Medline Urology Robotic Procedure Packs Recalled Due to Catheter Surface Contamination
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. UROLOGY ROBOTIC PROCEDURE PACK DYNJ0945779U
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0716-2026·2026-07-29
Rohto Cooling Eye Drops Max Strength Recalled Due to Sterility Concerns
Rohto-Mentholatum (Vietnam) Co., Ltd. is recalling Rohto Cooling Eye Drops Max Strength because there is a lack of assurance regarding the product's sterility.
Product
Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 90, 0.2%), Sterile 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742011012, NDC 10742-8158-1
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2793-2026·2026-07-29
SafeOp Patient Interface Neuromonitoring Device Recalled Due to Software Issue
Alphatec Spine, Inc. is recalling the SafeOp Patient Interface due to a software issue that may cause loss of electromyography functionality during surgery.
Product
SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2770-2026·2026-07-29
Penumbra System RED 68 Reperfusion Catheter Recall Due to Fracture Risk
Penumbra, Inc. is recalling its RED 68 Reperfusion Catheter due to manufacturing issues that may cause the device to fracture during use.
Product
Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0709-2026·2026-07-29
Levothyroxine Sodium Tablets Recalled Due to Subpotent Drug Concerns
Major Pharmaceuticals is voluntarily recalling certain lots of Levothyroxine Sodium Tablets (75 mcg) because the medication may be subpotent.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2757-2026·2026-07-29
Boston Scientific Steerable Sheath Recall Over Hemostatic Valve Damage
Boston Scientific is recalling its Faradrive Steerable Sheath devices due to potential hemostatic valve damage during preparation, which may cause air ingress and patient harm.
Product
FARADRIVE STEERABLE SHEATH CLEAR OUS, used to facilitate access to the vasculature and into the chambers of the heart, Material Number M004PFCE21M402, IFU Reference Number 51659727-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2784-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material Issues
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. ROBOTIC CDS980523M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2771-2026·2026-07-29
Boston Scientific TheraSphere 360 Y-90 Management Platform Software Recall Due to Calculation Error
Boston Scientific Corporation is recalling the TheraSphere 360 Y-90 Management Platform (Model M00139509001) due to a software anomaly that may cause incorrect dose calculations.
Product
Boston Scientific TheraSphere 360 Y-90 Management Platform, Model Number M00139509001; Radiological Image Processing System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2777-2026·2026-07-29
Emano Flow Uroflowmetry App Recalled Over Biased Flow Estimates
Emano Metrics is recalling 685 units of the Emano Flow smartphone-based acoustic uroflowmetry app (v2.0.0) because recordings captured at 48,000 Hz were processed by models trained on 44,100 Hz audio, producing systematically biased urinary flow rate and voided volume estimates.
Product
Emano Flow with software version v2.0.0 GS1 GTIN code: 199874903484 Emano Flow is a smartphone-based acoustic uroflowmetry system. Software-only device that measures urinary flow rate and voided volume from the acoustic signal of urination. No physical components. Distributed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0726-2026·2026-07-29
Lidocaine Injection Recall Due to Hair Contamination
Fresenius Kabi is recalling lidocaine injection vials after hair was found in the product. The recall affects 181,225 vials distributed nationwide.
Product
LIDOCAINE — LIDOCAINE (LIDOCAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2778-2026·2026-07-29
MiniMed Go App Recalled Due to Missed Insulin Alerts
Medtronic is recalling its MiniMed Go app because a software bug can prevent insulin dose alerts during nighttime, potentially leading to missed doses and hyperglycemia.
Product
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0728-2026·2026-07-29
Xylocaine Injection Recall Due to Hair Contamination
Fresenius Kabi is recalling 93,250 vials of Xylocaine (lidocaine HCl) injection due to the presence of particulate matter, specifically hair found in the product.
Product
XYLOCAINE — XYLOCAINE (LIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2755-2026·2026-07-29
FARADRIVE STEERABLE SHEATH CLEAR Medical Device Recall
Boston Scientific recalls FARADRIVE STEERABLE SHEATH CLEAR due to valve damage risk that could cause air embolism during heart procedures.
Product
FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21M402, IFU Reference Number LBL1062
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0710-2026·2026-07-29
Levothyroxine Sodium Tablets Recalled Due to Subpotent Drug Concerns
Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium Tablets (125 mcg) because the medication may be subpotent.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2787-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Contamination
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116G
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0701-2026·2026-07-29
Levothyroxine Sodium Tablets Recalled for Subpotency by Major Pharmaceuticals
Major Pharmaceuticals is voluntarily recalling Levothyroxine Sodium Tablets (50 mcg) from lot N02200 due to subpotency, meaning the tablets may contain less active ingredient than labeled. Products were distributed nationwide in the USA.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2780-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. DAVINCI PROSTATE PACK DYNJ68477L DYNJ68477M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0722-2026·2026-07-29
Rohto Cooling Eye Drops Recalled Due to Lack of Assurance of Sterility
Rohto-Mentholatum (Vietnam) Co., Ltd. is recalling certain lots of Rohto Cooling Eye Drops because the company cannot assure the sterility of the product.
Product
ROHTO — ROHTO (NAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2785-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Contamination
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. RR-DAVINCI PROSTATE ACCESSORY DYNJ63392F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2782-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. NON MB DAVINCI LITHOTOMY SM PK DYNJT6105
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2786-2026·2026-07-29
Medline Convenience Kits Containing Bard Silastic Foley Catheters Recalled Due to Surface Material
Medline Industries, LP is recalling 980 Medline convenience kits containing Bard Silastic Foley Catheters because excess raw material on the catheter surface may be harmful.
Product
Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. SM-LAPAROSCOPIC PROSTATE PAC DYNJ61206J
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0717-2026·2026-07-29
ROHTO Cooling Eye Drops Recalled Over Sterility Assurance Concerns
Rohto-Mentholatum is recalling ROHTO Cooling Eye Drops due to lack of assurance of sterility. The recall affects 499,673 cartons distributed nationwide in the U.S.
Product
Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0.03%, polysorbate 80 0.2%), Sterile, TWIN PACK, 0.4 FL OZ (13 mL), Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742011210, NDC 10742-8158-2
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·26E050000·2026-07-29
Toyota Recalls Side Curtain Air Bag Assemblies for Tacoma Vehicles
Toyota is recalling side curtain air bag assemblies for 2016-2023 Tacoma vehicles because they may be improperly secured, increasing injury risk during a crash.
Product
AIR BAGS:SIDE/WINDOW:CURTAIN recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0711-2026·2026-07-29
LEVOTHYROXINE SODIUM Tablets Recalled Due to Subpotent Drug Content
Major Pharmaceuticals is recalling LEVOTHYROXINE SODIUM 150 mcg tablets because some batches contain less active ingredient than labeled, potentially reducing thyroid hormone effectiveness.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide