State

Alabama product recalls

73,827 recalls have nationwide distribution and so reach Alabama. 6,378 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,378
Critical: 1,129
Severe: 1,605
Most recent: 2026-11-04

Of the 6,378 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,605 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50551–50575 of 80205

HighFDA (Devices)·Z-0061-2017·2016-10-19
Siemens Symbia S Camera Systems Recalled for Bearing Failure Risk
Siemens Medical Solutions is recalling Symbia S camera systems because linear bearing cars may fail, allowing ball bearings to fall out.
Product
Symbia S, Product Usage 1) SPECT: To Detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588 keV. 2) CT: The CT component is intended…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0069-2017·2016-10-19
Cardinal Health Recalls V. Mueller Spinal Distraction Screws Due to Corrosion
Cardinal Health 200, LLC is recalling V. Mueller Neuro/Spine Shadow-Line Spinal Distraction Screws because corrosion was demonstrated on the screw surface.
Product
V. Mueller Neuro/Spine, SHADOW-LINE, SPINAL DISTRACTION SCREW, STERILE, various sizes (12mm, 14mm, 16mm and 18mm) 5 PER BOX.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0081-2017·2016-10-19
Siemens Recalls Rubella IgM Assay Kits Due to False Positive Results
Siemens is recalling specific lots of Rubella IgM assay kits because they may produce false positive or indeterminate results on certain analyzers.
Product
SIEMENS IMMULITE/IMMULITE 1000 Systems Rubella IgM (RUM), REF/Catalog Number LKRM1 (OUS), Siemens Material Number (SMN) 10381282 (OUS), Unique Device Identification Number (UDI) 00630414964577; IVD --- For in vitro diagnostic use with the IMMULITE/IMMULITE 1000/IMMULITE…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0082-2017·2016-10-19
Siemens Rubella IgM Assay Recalled for False Positive Results
Siemens is recalling specific lots of Rubella IgM assays due to increased false positive and indeterminate results.
Product
SIEMENS IMMULITE/IMMULITE 2000 Systems Rubella IgM (RUM), REF/Catalog Number for US: L2KRM2(D), Siemens Material Number (SMN) for US: 10374021, REF/Catalog # for OUS: L2KRM2, SMN for OUS: 10381327; Unique Device Identification Number (UDI) 00630414961996; IVD --- For in vitro…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0070-2017·2016-10-19
Medtronic O-arm O2 Surgical Imaging System Recalled for Calibration Errors
Medtronic is recalling 14 O-arm O2 Surgical Imaging Systems because spatial calibration may be erroneous in navigated images, potentially affecting surgical accuracy.
Product
Medtronic Navigation O-arm O2 Surgical Imaging System Product Catalog Number: BI-700-02000 Product Usage: The O-arm Surgical Imaging System is a multi-dimensional surgical imaging platform that is designed for use in spine, orthopaedic, and trauma-related surgeries. It…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0056-2017·2016-10-19
Gold Standard Baking Recalls Cheese Decadent Danish Due to Metal Shavings
Gold Standard Baking is recalling Cheese Decadent Danish products because they may contain small metal shavings.
Product
Cheese Decadent Danish | NET WT 14 OZ (397g) | Gold Standard Baking, Chicago, IL 60632 | UPC: 087745050019
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0085-2017·2016-10-19
ConMed Recalls HeatWave Electrodes Due to Insulation Damage Risk
ConMed is recalling specific HeatWave Electrodes because damaged shaft insulation could increase the risk of patient burns during arthroscopic procedures.
Product
CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter, REF/Catalog Number CS-023, STERILE, Rx Only Product Usage: The HeatWave Electrode is intended to be used for electro-coagulation of soft tissue in shoulder, ankle, wrist, elbow and knee arthroscopic procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0061-2017·2016-10-19
Archer Farms Strawberry Danish Recalled for Metal Shavings
Gold Standard Baking is recalling Archer Farms Strawberry Danish due to the presence of small metal shavings.
Product
Archer Farms Strawberry Danish | NET WT 14 OZ (397g) | Distributed by Target Corporation Minneapolis, MN 55403 | UPC 085239101094
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0052-2017·2016-10-19
Publix Apple Strip Danish Recalled for Metal Shavings
Gold Standard Baking is recalling Publix Apple Strip Danishes due to the presence of small metal shavings.
Product
Publix Apple Strip Danish | Count, 1 | NET WT 15.00 oz | Distributed by Publix Supermarkets, Inc., Lakeland, FL 33802
Category
Food
Distribution
Distributed nationwide
HighNHTSA·16V757000·2016-10-19
Johnston VT651 and VT801 Street Sweepers Recalled for Hopper Detachment Risk
Johnston is recalling 2013-2016 VT651 and VT801 street sweepers because tipping hinges may crack, allowing the hopper to detach and increase injury risk.
Product
JOHNSTON — JOHNSTON VT801, VT651
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0057-2017·2016-10-19
Gold Standard Baking Recalls Cherry Decadent Danish Due to Metal Shavings
Gold Standard Baking is recalling Cherry Decadent Danish products due to the presence of small metal shavings. The recall covers 461 cases distributed nationwide.
Product
Cherry Decadent Danish | NET WT 14 OZ (397g) | Gold Standard Baking, Chicago, IL 60632 | UPC: 087745050033
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0056-2017·2016-10-19
Natus Medical Recalls Medix NatalCare LX Incubators Due to Wheel Defect
Natus Medical is recalling 104 Medix NatalCare LX Intensive Care Incubators because a defective base weld may cause wheels to bend out of alignment.
Product
The Medix NatalCare LX Intensive Care Incubator. Neonatal incubator. Item numbers: DMNCLX1; KITNC-STLX0003; KITNC-STLX0006; and KITNC-STLX0007.
Category
Medical Device
Distribution
15 states
HighFDA (Food)·F-0062-2017·2016-10-19
Gold Standard Baking Recalls Cheese Danish for Metal Shavings
Gold Standard Baking is recalling The Bakery Cheese Danish sold at Walmart due to the presence of small metal shavings.
Product
The Bakery Cheese Danish | Net Wt 14 OZ (397g) | Distributed By WAL-MART Stores, Inc, Bentonville, AR 72716 | UPC: 605388124487
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0060-2017·2016-10-19
Archer Farms Cheese Danish Recalled for Metal Shavings
Gold Standard Baking is recalling Archer Farms Cheese Danish due to the presence of small metal shavings.
Product
Archer Farms Cheese Danish | NET WT 14 OZ (397g) | Distributed by Target Corporation Minneapolis, MN 55403 | UPC 085239101094
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0059-2017·2016-10-19
Kroger Raspberry Danish Strips Recalled for Metal Shavings
Gold Standard Baking is recalling Kroger Raspberry Danish Strips due to the presence of small metal shavings.
Product
Kroger Raspberry Danish Strip, Naturally and Artificially Flavored | NET WT 14 OZ (396g) | Distributed by The Kroger Co., Cincinnati, Ohio 45202 | UPC: 011110836489
Category
Food
Distribution
Distributed nationwide
HighNHTSA·16V756000·2016-10-19
Newmar Recalls 2017 King Aire Motorhomes Due to Radar Mounting Defect
Newmar is recalling 2017 King Aire motorhomes because the collision mitigation radar may be mounted upside down, potentially decreasing performance and increasing crash risk.
Product
NEWMAR — NEWMAR KING AIRE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0065-2017·2016-10-19
Gold Standard Baking Recalls Apple Crumb Coffee Cake Due to Metal Shavings
Gold Standard Baking is recalling The Bakery Apple Crumb Coffee Cake because it may contain small metal shavings.
Product
The Bakery Apple Crumb Coffee Cake| Net Wt 15 OZ (425g) | Distributed By WAL-MART Stores, Inc, Bentonville, AR 72716 | UPC: 078742052953
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0048-2017·2016-10-19
Pharmedium Heparin Syringes Recalled Due to Potential Loss of Potency
Pharmedium Services, LLC is recalling 240 Heparin Sodium syringes because stability data does not support the expiry date, posing a risk of reduced drug potency.
Product
HEPARIN Sodium Inj., USP, 5,000 USP Heparin Units per 5 mL Total Volume in a syringe, NOT FOR LOCK FLUSH, 1,000 USP Heparin Units per mL, Rx only, PharMEDium, Product code 2K1925.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0071-2017·2016-10-19
Pharmedium Recalls Methadone Syringes Due to Potential Loss of Potency
Pharmedium Services, LLC is recalling 200 syringes of methadone HCl because stability data does not support the expiration dates, posing a risk of reduced drug potency.
Product
methadone HCl, 2.5 mg per 0.5 mL, in 0.9% Sodium Chloride, 0.5 mL Total Volume in a syringe, For IV Use Only, Rx only, PharMEDium, Product code 2T6134.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0084-2017·2016-10-19
Pharmedium Recalls Neostigmine Methylsulfate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 700 syringes of neostigmine methylsulfate because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
neostigmine Methylsulfate, 1 mg per mL, 3 mg per 3 mL, 3 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3551.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0047-2017·2016-10-19
Pharmedium Recalls Heparin Sodium Injections Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 399 syringes of Heparin Sodium Injection because stability data does not support the expiration dates, posing a risk of loss of potency.
Product
HEPARIN Sodium Inj. USP, 15,000 USP Heparin Units per 3 mL Injection 3 mL Total Volume in a syringe, Rx only, PharMEDium, Product code 2K1210.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0031-2017·2016-10-19
Pharmedium Recalls ePHEDrine Sulfate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 1,545 syringes of ePHEDrine Sulfate because stability data does not support the expiration dates, posing a risk of reduced potency.
Product
ePHEDrine Sulfate, 10 mg per mL, in 0.9% Sodium Chloride, Preservative Free, 1 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3347.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0083-2017·2016-10-19
Zimmer Biomet Recalls Phoenix Recon Soft Tissue Sleeve Guide Instruments
Zimmer Biomet is recalling 31 Phoenix Recon Soft Tissue Sleeve Guides due to incompatibility with new revision targeting arms, which may cause surgical delays.
Product
Phoenix Recon Soft Tissue Sleeve Guide, Surgical, Instrument for the sleeve and Orthopedic Manual Surgical Instruments for the Arm Product Usage: The Phoenix Femoral Nail System is to be implanted into the femur for alignment, stabilization and fixation of fractures caused…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0079-2017·2016-10-19
Pharmedium Recalls Morphine Sulfate Syringes Due to Stability Data Concerns
Pharmedium Services, LLC is recalling 21,506 syringes of morphine sulfate because stability data does not support the expiry dates, posing a risk of potency loss.
Product
morphine Sulfate, 1 mg per mL (2 mg per 2 mL), in 0.9% Sodium Chloride, Preservative Free (Contains Sulfites), 2 mL Total Volume in a syringe, For IV use, Rx only, PharMEDium, Product code 2R3259.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0053-2017·2016-10-19
Pharmedium Recalls Ketamine Syringes Due to Potential Loss of Potency
Pharmedium Services, LLC is recalling 25 syringes of ketamine HCl because stability data does not support the expiry date, posing a risk of reduced drug potency.
Product
ketamine HCl, 10 mg per mL, 50 mg per 5 mL, in 0.9% Sodium Chloride, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3234.
Category
Drug
Distribution
Distributed nationwide