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.

36001–36025 of 80118

SevereFDA (Drugs)·D-1411-2019·2019-07-03
Premier Pharmacy Labs Recalls Atropine Sulfate Injection Due to Sterility Concerns
Premier Pharmacy Labs is recalling 745 syringes of Atropine Sulfate Injection because FDA inspections found insufficient environmental controls that may compromise sterility.
Product
Atropine Sulfate PF INJ, 0.8 mg/2 mL (0.4 mg/mL), 2mL Single Dose Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-131-12, barcode 0 69623 13112 6.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1210-2019·2019-07-03
Becton Dickinson Recalls SmartSite Syringe Administration Sets Due to Leaking
Becton Dickinson is recalling SmartSite Syringe Administration Sets because they may leak, potentially interrupting infusions or exposing healthcare workers to fluids.
Product
SmartSite Syringe Administration Set-Product Package Size 50, Catalog Number: 10798696
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1433-2019·2019-07-03
Pramipexole Dihydrochloride Tablets Recalled for GMP Deviations and Cross-Contamination Risk
American Health Packaging is recalling Pramipexole Dihydrochloride Tablets due to GMP deviations and a cleaning procedure failure that may have caused cross-contamination.
Product
Pramipexole Dihydrochloride Tablets, 0.5 mg, 30 Tablets (6 tablets per blister card), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC Blister Card: 68084-974-95; NDC Carton: 68084-974-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1430-2019·2019-07-03
Diphenhydramine Liquid Recalled for Potential Microbial Contamination
H J Harkins Company is recalling Diphenhydramine HCL Liquid due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
Product
Diphenhydramine HCL Liquid, 12.5 mg/5 mL, 4 oz bottle, Manufactured by Torrent Pharma, Inc., Levittown, PA 19057, NDC 52959-0123-03.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1422-2019·2019-07-03
Premier Pharmacy Labs Recalls Neostigmine Methylsulfate Syringes for Sterility Concerns
Premier Pharmacy Labs is recalling Neostigmine Methylsulfate syringes nationwide due to FDA findings of insufficient environmental controls and lack of sterility assurance.
Product
Neostigmine Methylsulfate, 5mg/5mL (1mg/mL), 5mL Single Dose Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-234-15, barcode 5 69623 23415 0.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1423-2019·2019-07-03
Premier Pharmacy Labs Recalls Orphenadrine Citrate Syringes Due to Sterility Concerns
Premier Pharmacy Labs is recalling 4,363 syringes of Orphenadrine Citrate Sterile Injectable Solution because FDA inspections found insufficient environmental controls that may compromise sterility.
Product
Orphenadrine Citrate Sterile Injectable Solution *Contains Sulfites*, 30mg/mL, 1mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-104-10, barcode 7 69623 10410 5.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1888-2019·2019-07-03
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer Recalled for Bleeding Risk
Ethicon Endo-Surgery Inc is recalling ENSEAL X1 Curved Jaw Tissue Sealers due to reported intraoperative bleeding.
Product
Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 25cm Shaft PRODUCT CODE: NSLX125C
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V513000·2019-07-03
BMW Recalls Multiple Models for High Pressure Fuel Pump Defect
BMW is recalling specific 2019-2020 models because a high pressure fuel pump may not be properly attached, potentially causing a fuel leak and fire risk.
Product
BMW — BMW X5, M850I, X7, 750I
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1413-2019·2019-07-03
Premier Pharmacy Labs Recalls Chlorpromazine Injection Due to Sterility Concerns
Premier Pharmacy Labs is recalling 824 vials of Chlorpromazine HCL Injection because an FDA inspection found insufficient environmental controls that may compromise sterility.
Product
ChlorproMAZINE HCL INJ, 25mg/mL, *Contains Sulfites*, 1mL in a 5mL Sterile SDV, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-122-28, barcode 7 69623 12228 4.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1415-2019·2019-07-03
Premier Pharmacy Labs Recalls Droperidol Syringes Due to Sterility Concerns
Premier Pharmacy Labs is recalling 2,315 syringes of Droperidol Injectable Sterile Solution because FDA inspections found insufficient environmental controls and lack of sterility assurance.
Product
Droperidol Injectable Sterile Solution, 0.625mg/mL, 1mL in a 3mL Sterile Single-Use Syringe, Rx only, Premier Pharmacy Labs, 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-185-10, barcode 0 69623 18510 5.
Category
Drug
Distribution
Distributed nationwide
HighCPSC·19757·2019-07-03
The Company Store Recalls Girls' Pajama Sets for Flammability Violation
The Company Store is recalling about 2,500 girls' pajama sets because they fail to meet federal flammability standards, posing a burn risk.
Product
Girl's pajama sets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1879-2019·2019-07-03
GE Healthcare Recalls Replacement ECG Leadwires Due to Defibrillation Risk
GE Healthcare is recalling 58,045 replacement ECG leadwires worldwide because they may reduce energy delivery during defibrillation, potentially limiting the success of the procedure.
Product
Replacement ECG leadwires with snap ends REF/Catalog Number Description 2106386-101 Replacement ECG Leadwire, snap, LL, AHA, 130 cm/ 51 in The reusable ECG leadwire sets enable ECG monitoring with GE equipment requiring rectangular 11-pin ECG trunk cable. Use leadwire sets…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1784-2019·2019-07-03
Collins Aerospace TASE 500 Imaging Systems Recalled for Laser Safety Error
Collins Aerospace is recalling TASE 500 Imaging systems because the Nominal Ocular Hazard Distance for the alignment laser was miscalculated.
Product
TASE 500 Imaging systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1852-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk
Maquet is recalling two VOLISTA StandOP Surgical Lights because the light head coating may crack, posing a risk of particles falling into the surgical field.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811901 Model: VLT600SF AIM STP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1859-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk
Maquet is recalling 12 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, posing a risk of particles falling into the surgical field.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229002A Model: VST66SF AIM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1855-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled Due to Coating Crack Risk
Maquet is recalling 46 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, risking particle contamination in the surgical field.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811961 Model: VLT600DF AIM STP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1886-2019·2019-07-03
GE Healthcare Recalls Centricity Universal Viewer for Missing Image Warning
GE Healthcare is recalling 292 units of the Centricity Universal Viewer because it may fail to warn users when medical images are missing from exams.
Product
Centricity Universal Viewer with PACS-IW foundation 6.0, Model number 2090255-001 Product Usage: Centricity PACS-IW with Universal Viewer is a device that displays medical images (including mammograms) and data from various imaging sources. Images and data can be viewed…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V512000·2019-07-03
Winnebago Forza Motorhomes Recalled for Storage Door Defect
Winnebago is recalling 2017-2019 Forza motorhomes because the exterior storage compartment door may unexpectedly open while driving, increasing crash risk.
Product
WINNEBAGO — WINNEBAGO FORZA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1863-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk
Maquet is recalling 9 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, posing a risk of particles falling into the surgical field.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229036A Model:VST66SF
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1856-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk
Maquet is recalling 7 units of VOLISTA StandOP Surgical Lights because the coating on the light head forks may crack, posing a risk of particles falling into the surgical field.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568812910 Model: VLT400SF STP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1876-2019·2019-07-03
GE Healthcare Recalls ECG Leadwire Sets Due to Defibrillation Risk
GE Healthcare is recalling ECG leadwire sets because they may reduce energy reaching patients during defibrillation, potentially limiting treatment success.
Product
ECG leadwire sets: REF/Catalog Number Description 2106389-001 ECG Leadwire set, 5-lead, grouped, grabber, AHA, 74 cm/ 29 in 2106389-002 ECG Leadwire set, 5-lead, grouped, grabber, AHA, 130 cm/ 51 in 2106389-003 ECG Leadwire set, 5-lead, grouped, grabber, IEC, 74 cm/ 29 in…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19756·2019-07-03
Just Love Fashion Recalls Children's Pajama Pants for Flammability Violation
Just Love Fashion is recalling Prince of Sleep children's pajama pants because they fail federal flammability standards, posing a burn risk.
Product
Children's pajama pants
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1877-2019·2019-07-03
GE Healthcare Recalls ECG Leadwires Due to Defibrillation Energy Reduction
GE Healthcare is recalling 58,045 replacement ECG leadwires because they may reduce energy reaching patients during defibrillation, potentially limiting treatment success.
Product
Replacement leadwires with grabber ends: REF/Catalog Number Description 2106388-005 Replacement ECG Leadwire, grabber, BRN V, AHA, 74 cm/ 29 in 2106388-101 Replacement ECG Leadwire, grabber, LL , AHA, 130 cm/ 51 in 2106388-103 Replacement ECG Leadwire, grabber, GRN RL, AHA…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1854-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled Due to Coating Crack Risk
Maquet is recalling 65 VOLISTA StandOP Surgical Lights because the coating on the light head forks may crack, posing a risk of particles falling into the surgical field and causing patient infection.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811911 Model: VLT600SF AIM STP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1864-2019·2019-07-03
Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk
Maquet is recalling 10 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, potentially dropping particles into the surgical field.
Product
Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229037A Model: VST66DF
Category
Medical Device
Distribution
Distributed nationwide