State

Alabama product recalls

73,734 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 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31901–31925 of 80111

ModerateFDA (Devices)·Z-1575-2020·2020-04-01
BardPort Titanium Implantable Port Recall Due to Incorrect Catheter Tip
Bard Peripheral Vascular Inc is recalling 360 BardPort Titanium Implantable Ports because they may contain an incorrect catheter tip, potentially prolonging surgery.
Product
BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter , REF: 0602230, UDI: (01)00801741025563 Product Usage: Bard implantable ports are indicated for patient therapies requiring repeated access to the vascular system. The port system…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1579-2020·2020-04-01
Bard PowerFlow Apheresis IV Port Recalled for Incorrect Tunneler Tip
Bard Peripheral Vascular Inc is recalling 296 PowerFlow Implatable Apheresis IV Ports because they may contain an incorrect tunneler tip, potentially prolonging surgical operations.
Product
PowerFlow Implatable Apheresis IV Port with attachable 9.6 F ChronoFl x Open-Ended Single-Lumen Venous Catheter, Ref A710962, UDI:(01)00801741129438 Product Usage: Bard implantable ports are indicated for patient therapies requiring repeated access to the vascular system. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1537-2020·2020-04-01
Siemens Atellica CH Total Bilirubin Assay Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling Atellica CH Total Bilirubin assays because they may show inaccurate high results for patients taking eltrombopag.
Product
Atellica CH Total Bilirubin_2 assay-In vitro Diagnostic for the determination of total bilirubin SMN: 11097531 - Product Usage: Atellica TBil_2 assay is for in vitro diagnostic use in the quantitative determination of total bilirubin in human serum and plasma (lithium heparin)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1540-2020·2020-04-01
Siemens Total Bilirubin Reagent Cartridge Recall for Eltrombopag Interference
Siemens Healthcare is recalling Dimension Total Bilirubin Flex reagent cartridges because the assay may show falsely high results for patients taking eltrombopag.
Product
Dimension Total Bilirubin Flex reagent cartridge -In vitro Diagnostic for the determination of total bilirubin. SMN: 10444957 Product Usage: Dimension TBI method for the ¿ clinical chemistry syst6em is an in vitro diagnostic test intended to quantitatively measure total…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0900-2020·2020-04-01
Organic By Nature Recalls L.O.V.E. Supermeal Original Due to Unapproved Herbicide
Organic By Nature, Inc. is recalling L.O.V.E. Supermeal Original products because the organic ground flaxseed powder ingredient was found to contain the unapproved herbicide Haloxyfop.
Product
L.O.V.E. Supermeal Original: 420g Plastic Bottle, 1396g Plastic Bottle, 693g Bio Bag Terra Pouch; Finished Product Item # 2700E, 2711, 2712, 2712-P65 Platinum Health Europe, Netherlands, Purim Health Products, Rancho Dominguez, CA
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1544-2020·2020-04-01
Medline Stick Sponge Presaturated W/PVP Recalled for Packaging Seal Voids
Medline is recalling Stick Sponge Presaturated W/PVP units due to packaging seal voids that compromise sterility.
Product
Medline Stick Sponge Presaturated W/PVP REF DYND70288 DYND70288H 2/PK Expiration 06/30/2022.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1536-2020·2020-04-01
Siemens Atellica CH Direct Bilirubin Assay Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling Atellica CH Direct Bilirubin assays because they may show inaccurate results for patients taking eltrombopag.
Product
Atellica CH Direct Bilirubin_2 assay In vitro Diagnostic for the determination of direct bilirubin SMN: 11097532 - Product Usage: ADVIA DBIL_ 2 is for in vitro diagnostic use in the quantitative determination of direct bilirubin in human serum and plasma on the ADVIA¿ Chemistry…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1573-2020·2020-04-01
Bard Vaccess CT Implantable Port Recall Due to Incorrect Tunneler Tip
Bard Peripheral Vascular Inc is recalling 598 Vaccess CT Power-Injectable Implantable Ports because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgical operations.
Product
1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs, Ref: 7496000, UDI:(01)00801741027482 Product Usage: Bard implantable ports are indicated for patient therapies requiring repeated access to the vascular system. The port system can be used for infusion of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0905-2020·2020-04-01
Touchstone Essentials Super Greens Juice Recalled for Unapproved Herbicide
Organic By Nature, Inc. is recalling Touchstone Essentials Super Greens Juice due to the presence of the unapproved herbicide Haloxyfop in an ingredient.
Product
Touchstone Essentials Super Greens Juice - Raspberry Apple; Premium Organic Superfood Juice Powder: Whole Food Dietary Supplement; Net Wt. 10.5 oz. (300 g) Plastic Bottle; Finished Product Item#: FTSGJRA300G Manufactured Exclusively for: Touchstone Essentials, Raleigh…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1571-2020·2020-04-01
Bard PowerPort M.R.I. Implantable Port Catheter Recall for Incorrect Tunneler Tip
Bard Peripheral Vascular Inc is recalling 878 PowerPort M.R.I. Implantable Port catheters because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgical operations.
Product
1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter with Suture Plugs, REF: 1809600, UDI: (01)00801741027130 ; 2. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter Without Suture…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0898-2020·2020-04-01
Organic By Nature Daily Fiber Blend Recalled for Unapproved Herbicide
Organic By Nature is recalling Daily Fiber Blend - Caramel Apple Flavor because the flaxseed powder ingredient contains unapproved herbicide Haloxyfop.
Product
Daily Fiber Blend - Caramel Apple Flavor; Organic Plant Powder Mix for preparation of a fiber-rich drink, 540g Plastic Bottle, 180g Bio Bag Terra Pouch; Finished Product Item#: 2012E, 2012, 2012-P65, 2013, 2013-P65, 2016, 2016-P65 Brand names of: Platinum Health Europe…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1577-2020·2020-04-01
BardPort M.R.I. Hard Base Implantable Port Recall Due to Incorrect Tunneler Tip
Bard Peripheral Vascular Inc is recalling 151 BardPort M.R.I. Hard Base Implantable Ports because they may contain an incorrect tunneler barb tip, potentially prolonging surgical operations.
Product
BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter, Ref: 0604550, UDI: (01)00801741025860 Product Usage: Bard implantable ports are indicated for patient therapies requiring repeated access to the vascular system. The port…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0895-2020·2020-04-01
Organic By Nature Chia/Flax Boost Recalled for Unapproved Herbicide
Organic By Nature is recalling Chia/Flax Boost dietary supplements because the flaxseed powder contains unapproved herbicide Haloxyfop.
Product
care/of Chia/Flax Boost Dietary Supplement; Net Wt. 0.35 oz. (10g) foil packets; Finished Product Item # FCOFBP10G Distributed by Noho Health Inc., New York, NY 10013
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1529-2020·2020-04-01
Fresenius Medical Care Recalls Honeywell Pressure Transducers for Hemodialysis Systems
Fresenius Medical Care is recalling 3,561 Honeywell pressure transducers used in hemodialysis delivery systems due to lower long-term reliability.
Product
Honeywell Pressure Transducer- Part Number: 370506-22. It is a component used in 2008T, Common Name: Hemodialysis Delivery System; 2008T HD SYS. BLUE STAR; 2008K2, Common Name: Hemodialysis Delivery Equipment; 2008K@home, Common Name: Hemodialysis Delivery System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0901-2020·2020-04-01
Organic By Nature Supermeal Vanilla Chai Recalled for Unapproved Herbicide
Organic By Nature is recalling L.O.V.E. Supermeal Vanilla Chai because it contains Organic Ground Flaxseed powder contaminated with the unapproved herbicide Haloxyfop.
Product
L.O.V.E. Supermeal Vanilla Chai: 1320g Plastic Bottle, 660g Bio Bag Terra Pouch; Finished Product Item #: 2910E, 2910, 2910-P65, 2911, 2911-P65 Platinum Health Europe, Netherlands, Purim Health Products, Rancho Dominguez, CA
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1539-2020·2020-04-01
Siemens ADVIA Chemistry Total Bilirubin Assay Recalled for Positive Bias
Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Total Bilirubin assays because they may show falsely high results for patients taking eltrombopag.
Product
ADVIA Chemistry Total Bilirubin_2 assay- SMN: 10341115 (40 mL) & 10341113 (70 mL). Product Usage: ADVIA TBIL_2 is for in vitro diagnostic use in the quantitative determination of total bilirubin in human serum and plasma of adults and neonates on the ADVIA¿ Chemistry…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1578-2020·2020-04-01
Bard X-Port isp MRI Implantable Port Recall for Incorrect Tunneler Tip
Bard Peripheral Vascular Inc is recalling 225 X-Port isp MRI Implantable Ports because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgical operations.
Product
1. X-Port isp M.R.I Implantable Port, with Pre-Attached 9.6 F Open-Ended Single-Lumen Venous Catheter, REF:0607550, UDI:(01)00801741026195 2. X-Port isp M.R.I. Implantable Port, with Attachable 9.6F Open-Ended Single-Lumen Venous Catheter, REF: 0657525, UDI:(01)00801741026379…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1060-2020·2020-04-01
Nystatin Oral Suspension Recalled for Low Potency
Pharmaceutical Associates, Inc. is recalling Nystatin Oral Suspension because it tested below the required potency level.
Product
NYSTATIN — NYSTATIN (NYSTATIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0897-2020·2020-04-01
Nested Naturals Super Kids Powder Recalled for Unapproved Herbicide
Organic By Nature, Inc. is recalling Nested Naturals Super Kids powder because the flaxseed ingredient contains an unapproved herbicide.
Product
Nested Naturals Super Kids; Superfood Powder Full of Nutrients for Growing Bodies; Whole Food Powder, Net Wt. 7.5 oz (210g), 30 servings; Finished Product Item # FNNKFMSG210G; Bulk Finished Product Item # FGBPNNKFMSG Distributed by Nested Naturals Vancouver, BC, Canada
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1547-2020·2020-04-01
Randox Chemistry QC Premium Plus Recalled for Incorrect Sodium Values
Randox Laboratories is recalling Chemistry QC Premium Plus due to incorrect Sodium target values. The error affects quality control accuracy for diagnostic assays.
Product
Chemistry QC Premium Plus, Cat. No. LAL4213, GTIN 05055273209006 - Product Usage: This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The device is for the control of accuracy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0894-2020·2020-04-01
Alkamind Creamy Vanilla Organic Daily Protein Recalled for Unapproved Herbicide
Organic By Nature, Inc. is recalling Alkamind Creamy Vanilla Organic Daily Protein because the flaxseed powder ingredient contains unapproved herbicide Haloxyfop.
Product
Alkamind Creamy Vanilla Organic Daily Protein; 450g Plastic Bottle; Finished Product Item # FAMVDP450G; 3 core alkaline proteins Distributed by Alkamind LLC, New York, NY 10028
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1541-2020·2020-04-01
Siemens Dimension Vista Total Bilirubin Reagent Cartridge Recall
Siemens Healthcare Diagnostics is recalling Dimension Vista Total Bilirubin reagent cartridges because they may produce inaccurate results for patients taking eltrombopag.
Product
Dimension Vista¿ Total Bilirubin Flex¿ reagent cartridge -In vitro Diagnostic for the determination of total bilirubin. SMN: 10445146 Product Usage: Dimension Vista TBIL method is an in vitro diagnostic test intended to quantitatively measure total bilirubin in human…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0896-2020·2020-04-01
Organic By Nature Slim Natural Raw Meal Recalled for Unapproved Herbicide
Organic By Nature is recalling Slim Natural Raw Meal due to the presence of unapproved herbicide Haloxyfop in the flaxseed powder.
Product
Erom, Inc. Slim Natural Raw Meal; Bulk; Finished product item # FGBPEIOS-E
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1599-2020·2020-04-01
Siemens Atellica CH Ethyl Alcohol Assay Recalled for Calibration Bias
Siemens Healthcare Diagnostics is recalling Atellica CH Ethyl Alcohol assays due to potential positive bias in results within the 10-day calibration interval.
Product
Atellica CH Ethyl Alcohol, Test Code ETOH, Siemens Material Number (SMN) 11097501, UDI 00630414596112. The product is an ethyl alcohol assay, IVD use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0902-2020·2020-04-01
Organic By Nature Recalls RAWr! Life Superfoods Due to Unapproved Herbicide
Organic By Nature is recalling RAWr! Life Organic Superfoods because the flaxseed powder ingredient contains an unapproved herbicide.
Product
RAWr! Life Organic Superfoods; Dietary Supplement; 300g Plastic Bottle (10.60 oz.); Finished Product Item # FHEEG300G Rawr! Life, Glendale, AZ 85308
Category
Food
Distribution
Distributed nationwide