State

Alabama product recalls

73,741 recalls have nationwide distribution and so reach Alabama. 6,377 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total: 6,377
Critical: 1,129
Severe: 1,604
Most recent: 2026-10-28

Of the 6,377 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 1,604 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38426–38450 of 80118

HighFDA (Devices)·Z-0825-2019·2019-02-20
Hemotherm CE Dual Reservoir Cooler/Heater Recalled for Overheating Risk
Cincinnati Sub-Zero is recalling 396 Hemotherm CE Dual Reservoir Cooler/Heater units because fuse clips may stretch, causing overheating and device shutdown.
Product
Hemotherm CE Dual Reservoir Cooler/Heater, Model No. 400CE Product Usage: The HEMOTHERM¿ Model 400CE Dual Reservoir Cooler/Heater is used to lower, maintain, or raise the temperature of the water flowing through a Blood Oxygenator / Heat Exchanger that is used to cool or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0834-2019·2019-02-20
Signature Orthopedics Recalls Three Genius Knee Cemented CR Femoral Components
Signature Orthopedics is voluntarily recalling three Genius Knee Cemented CR Femoral Components due to a product mix-up. The devices were distributed in Florida, New York, and Tennessee.
Product
Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement component
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0885-2019·2019-02-20
RXBAR Recalls Mango Pineapple Bars Due to Undeclared Peanut Allergen
Chicago Bar Company LLC is voluntarily recalling RXBAR Mango Pineapple bars because they contain undeclared peanut, a major food allergen.
Product
RXBAR: Mango Pineapple,1.83oz bars, single bar, 12-count carton, 4- count carton
Category
Food
Distribution
43 states
HighFDA (Food)·F-0879-2019·2019-02-20
RXBAR Recalls Chocolate Sea Salt Bars Due to Undeclared Peanut
Chicago Bar Company LLC is voluntarily recalling Chocolate Sea Salt RXBARs because they contain undeclared peanut, a major food allergen.
Product
Chocolate Sea Salt RXBARs , 1.83 oz., single bar, , 12-count carton, 10-count carton, , 5-count carton, 4-count carton
Category
Food
Distribution
43 states
HighFDA (Food)·F-0886-2019·2019-02-20
RXBAR Maple Sea Salt Bars Recalled for Undeclared Peanut Allergen
Chicago Bar Company LLC is voluntarily recalling RXBAR Maple Sea Salt bars due to an undeclared peanut allergen.
Product
RXBAR: Maple Sea Salt, 1.83 oz bars, single bar, 2-count carton, 4-count carton
Category
Food
Distribution
43 states
HighFDA (Food)·F-0881-2019·2019-02-20
RXBAR Blueberry Bars Recalled for Undeclared Peanut Allergen
Chicago Bar Company LLC is voluntarily recalling RXBAR Blueberry bars due to the presence of undeclared peanut, a major food allergen.
Product
RXBAR:Blueberry, 1.83oz bars, single bar, 12-count carton, , 10-count carton, , 5-count carton, , 4-count carton
Category
Food
Distribution
43 states
ModerateFDA (Drugs)·D-0997-2019·2019-02-20
Avella Recalls Labetalol Syringes Due to Incorrect Barcode Expiration Dates
Avella of Deer Valley, Inc. is recalling 2,840 syringes of Labetalol 20mg Injectable Solution because the 2D barcodes contain incorrect expiration dates.
Product
Labetalol 20mg, HCL, USP Injectable Solution, 20mg/4mL (5 mg per mL), 4mL single use syringe. Repackaged by Avella Specialty Pharmacy 24416 N 19th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-822-71.
Category
Drug
Distribution
13 states
ModerateFDA (Drugs)·D-0999-2019·2019-02-20
Avella Recalls Magnesium Sulfate Bags Due to Incorrect Barcode Expiration Dates
Avella of Deer Valley is recalling 4,950 bags of compounded magnesium sulfate because the 2D barcodes contain incorrect expiration dates that do not match the label.
Product
MAGnesium 2gm sulfate, added to D5W 50 mL, Volume: 54 mL, Sterile single use bag, Compounded by Avella Specialty Pharmacy 24416 N 19th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-902-05.
Category
Drug
Distribution
13 states
ModerateFDA (Devices)·Z-0823-2019·2019-02-20
Philips Ingenuity TF PET/CT Software Update Corrects Multiple Issues
Philips is issuing a software update for 24 Ingenuity TF PET/CT systems to correct multiple issues identified in the previous software version.
Product
Ingenuity TF PET/CT (non-RoHS), Model Number 882456 This device is a diagnostic imaging system that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem produces cross-sectional images of the body by computer reconstruction…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0826-2019·2019-02-20
Ottobock PushValve Recall for Diameter Specification Defect
Ottobock is recalling 538 PushValve units because some valve inserts have a diameter smaller than the specification. The valve is used for prosthetic fitting of lower limb amputees.
Product
21Y14 PushValve Product Usage: The PushValves/ MagValves is intended exclusively for the prosthetic fitting of lower limb amputees. The valve is a threadless one-way valve. It is used to evacuate air from the prosthetic socket.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0489-2019·2019-02-20
Valeant Recalls Cardizem CD Capsules for Dissolution Failures
Valeant Pharmaceuticals is recalling 390 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, potentially affecting drug release.
Product
CARDIZEM CD — CARDIZEM CD (DILTIAZEM HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0833-2019·2019-02-20
Signature Orthopedics Recalls Genius Knee Cemented Tibial Components Due to Product Mix-Up
Signature Orthopedics is recalling 10 Genius Knee Cemented Tibial Components due to a product mix-up. The recall covers units distributed in Florida, New York, and Tennessee.
Product
Genius Knee Cemented Tibial Component Product Usage: Knee replacement component
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0482-2019·2019-02-20
US Compounding Recalls LET Gel 4% Syringes Due to Missing Lot and Expiration Dates
US Compounding Inc is recalling 1,931 syringes of LET Gel 4% because the labels are missing specific lot and expiration dates.
Product
LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 0.05% + Tetracaine HCl 0.5%), 3mL Single Use Syringe, Rx only, US Compounding, 1270 Don's Lane, Conway, AR, 800-718-3588, Barcode 62295501303.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0490-2019·2019-02-20
Valeant Recalls Cardizem CD Capsules for Dissolution Failures
Valeant Pharmaceuticals is recalling 22 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, potentially affecting drug release.
Product
CARDIZEM CD — CARDIZEM CD (DILTIAZEM HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0828-2019·2019-02-20
Ottobock MagValve Recall for Prosthetic Socket Air Evacuation Defect
Ottobock is recalling 110 MagValve units used in prosthetic sockets because some valve inserts have a smaller diameter than specified.
Product
21Y15 MagValve Product Usage: The PushValves/ MagValves is intended exclusively for the prosthetic fitting of lower limb amputees. The valve is a threadless one-way valve. It is used to evacuate air from the prosthetic socket.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0488-2019·2019-02-20
Valeant Recalls Cardizem CD Capsules for Dissolution Failures
Valeant Pharmaceuticals is recalling 206 bottles of Cardizem CD capsules because they failed to meet dissolution specifications, meaning the drug may not release properly.
Product
CARDIZEM CD — CARDIZEM CD (DILTIAZEM HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1000-2019·2019-02-20
Avella recalls magnesium sulfate bags with incorrect barcode expiration dates
Avella of Deer Valley is recalling 8,500 bags of compounded magnesium sulfate because the 2D barcodes contain incorrect expiration dates that do not match the label.
Product
MAGnesium 2 gm sulfate, added to NS 50 mL, Sterile single use bag, 54 mL, Compounded by Avella Specialty Pharmacy 24416 N 19 th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-907-05.
Category
Drug
Distribution
13 states
ModerateFDA (Devices)·Z-0827-2019·2019-02-20
Ottobock PushValve Upper Part Recalled for Diameter Specification Defect
Ottobock is recalling PushValve upper parts because some installed valve inserts have a diameter smaller than the specification.
Product
21Y14=S PushValve upper part Product Usage: The PushValves/ MagValves is intended exclusively for the prosthetic fitting of lower limb amputees. The valve is a threadless one-way valve. It is used to evacuate air from the prosthetic socket.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0998-2019·2019-02-20
Avella recalls magnesium sulfate bags with incorrect barcode expiration dates
Avella of Deer Valley is recalling 250 bags of compounded magnesium sulfate due to incorrect expiration dates in the 2D barcodes.
Product
MAGnesium 1gm sulfate, added to D5W 50 mL, Volume 52 mL, sterile single use bag, Compounded by Avella Specialty Pharmacy 24416 N 19th Avenue, Phoenix, AZ 85085 (877) 794-0404, NDC 42852-901-05.
Category
Drug
Distribution
13 states
ModerateFDA (Drugs)·D-0487-2019·2019-02-20
Valeant Recalls Cardizem CD Capsules for Dissolution Failures
Valeant Pharmaceuticals is recalling 1,023 bottles of Cardizem CD (diltiazem hydrochloride) 120 mg capsules because they failed to meet dissolution specifications.
Product
CARDIZEM CD — CARDIZEM CD (DILTIAZEM HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0491-2019·2019-02-20
Valeant Recalls Diltiazem HCl Capsules for Dissolution Failures
Valeant Pharmaceuticals is recalling 23,884 bottles of Diltiazem HCl CD capsules because they failed dissolution specifications, potentially affecting drug release.
Product
Diltiazem HCl CD capsules, 360 mg, 90-count bottles, Rx Only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807 USA; By: Valeant Pharmaceuticals International, Inc., Steinbach, MB R5G 1Z7 Canada; NDC…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0995-2019·2019-02-20
Dr. Reddy's Recalls Esomeprazole Magnesium Capsules Due to Discoloration
Dr. Reddy's Laboratories is recalling Esomeprazole Magnesium 40mg capsules because they may contain brown pellets.
Product
ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0483-2019·2019-02-20
Akorn Recalls COSOPT Ophthalmic Solution Due to Stability Failures
Akorn Inc. is recalling 30,794 bottles of COSOPT Ophthalmic Solution because the product failed stability specifications for opalescence.
Product
COSOPT Ophthalmic Solution, USP, (2% Dorzolamide Hydrochloride, 0.5% Timolol Maleate), 10 mL dropper bottle, Sterile, Rx only, Distributed by: Akorn, Inc., Lake Forest, IL, NDC: 17478-605-10
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0822-2019·2019-02-20
Luminex Recalls Verigene BC-GP Utility Kits Due to Labeling Error
Luminex Corporation is recalling Verigene BC-GP Utility Kits because they were incorrectly labeled with Amplification Tray labels.
Product
Vergene Amplification Tray - 700uL, BC-GP REF 20-011-018 The Verigene(R) Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) performed using the sample-to-result Verigene System is a qualitative, multiplexed in vitro diagnostic test for the simultaneous detection and…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V108000·2019-02-19
Keystone Recalls 2019 Crossroads Redwood Trailers Due to Pin Box Bolt Issue
Keystone is recalling 2019 Crossroads Redwood recreational trailers because insufficiently tightened pin box mounting bolts could cause the trailer to separate from the tow vehicle.
Product
CROSSROADS — CROSSROADS REDWOOD
Category
Vehicle
Distribution
Distributed nationwide