State

Alabama product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31451–31475 of 80099

HighFDA (Devices)·Z-1878-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Potential Seam Holes
Maquet is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175922P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1859-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Line Holes
Maquet Cardiovascular is recalling specific Hemashield Gold vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral, Product Code: M002020955010 - Product Usage: For use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1886-2020·2020-05-13
CME America Recalls BodyGuard Microset Infusion Sets Due to Filter Defect
CME America is recalling BodyGuard Microset infusion sets because the installed filter may have the incorrect pore size. The recall affects 30,300 units distributed nationwide.
Product
BodyGuard Microset For Use with the BodyGuard Infusion Pump *** Tubing: 110 in. (280 cm) - Blue Stripe - Product Usage: The system is intended for patients who require maintenance medications, PCA therapy, parenteral nutritional fluids, and general IV fluid therapy in hospital…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1872-2020·2020-05-13
Hemashield Platinum Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175828P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20120·2020-05-13
Hodedah Recalls 4-Drawer Chests Due to Tip-Over and Entrapment Hazards
Hodedah is recalling HI4DR 4-drawer chests because they may tip over or entrap children if not anchored to the wall.
Product
Hodedah HI4DR 4-drawer chests
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·20V269000·2020-05-13
2020–2021 Forest River Vibe Trailers Recalled for Missing Refrigerator Roof Vent
Forest River is recalling certain 2020–2021 Vibe trailers because the roof vent for the refrigerator may be missing. Without proper ventilation, the refrigerator could overheat and create a fire risk, or carbon monoxide could accumulate inside the trailer.
Product
FOREST RIVER — FOREST RIVER VIBE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1870-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Line Defects
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch, Product Code: M00202175824P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1926-2020·2020-05-13
Stryker Recalls Spy-Phi Drapes Packaged in Unsealed Pouches
Stryker is recalling 21,078 units of Spy-Phi Drapes because they were packaged in unsealed pouches, compromising sterility.
Product
Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally only). Drape/ UDI: HH2020/20858701006326
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1890-2020·2020-05-13
Intuitive Surgical Recalls daVinci XI Sureform Stapler Reloads Due to Deployment Defect
Intuitive Surgical is recalling 22,752 daVinci XI Sureform 60 reloads worldwide because a manufacturing variation may prevent adjacent staples from deploying, potentially causing an incomplete staple line.
Product
daVinci XI Sureform 60 reload, 60 mm Green 6- Row, 4.6 mm, REF 48360G-08, UDI: 00886874113844, Rx Only, Sterile EO - Product Usage: are intended to be used with da Vinci Surgical Systems for resection, transection, and, or creation of anastomoses in General, Thoracic…
Category
Medical Device
Distribution
Distributed nationwide
HighUSDA FSIS·010-2020·2020-05-13
Evans Food Group Recalls Pork Skin Products Due to Undeclared Soy
Evans Food Group is recalling ready-to-eat pork skin products because the variety pack label fails to declare soy, a known allergen.
Product
Evans Food Group — Evans Food Group Recalls Ready-To-Eat Pork Skin Products due to Misbranding
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1879-2020·2020-05-13
Maquet Hemashield Platinum Vascular Grafts Recalled for Seam Line Bleeding Risk
Maquet Cardiovascular is recalling Hemashield Platinum Woven Double Velour Vascular Grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175924P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1882-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Holes
Maquet Cardiovascular is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that may cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch, Product Code: M00202175930P0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1899-2020·2020-05-13
Varian Multileaf Collimator Recall Due to Software-Related Leaf Movement Failure
Varian Medical Systems is recalling 151 Multileaf Collimators because a software upgrade caused leaves to fail to move during specific arc treatments.
Product
Varian Multileaf Collimator [MLC]; Millenium Multileaf Collimator [52, 80, 120 leaf]; High Definition 120 Multileaf Collimator Model Number(s): product code: H54 and H56; MLC software version 8.5 - Product Usage: is intended to assist the clinician in the delivery of external…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1841-2020·2020-05-13
Philips Recalls Transesophageal Ultrasound Transducers Due to Temperature Measurement Failure
Philips Ultrasound Inc is recalling S7-3t transesophageal transducers because a manufacturing programming error prevents the system from correctly measuring tip temperature, which may stop auto-cooling and cause patient injury.
Product
Transducer S7-3t UDI (01)00884838061439 REF 989605406772 Can be used with: CX50, EPIQ 7, Affiniti 50 and Affiniti 70 Ultrasound systems - Product Usage: Diagnostic ultrasound imaging or fluid flow analysis of the human body - particularly transesophageal echocardiography…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1838-2020·2020-05-13
Ivoclar Vivadent recalls dental ceramic blocks due to cracking during sintering
Ivoclar Vivadent AG is recalling 332 units of IPS e.max ZirCAD ceramic blocks because they crack during the sintering process. The recall covers lots Y47472 and Z000V0 distributed nationwide.
Product
Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A2 C17/5 - ceramic for dental use,intended for IPS e.max ZirCAD presintered yttrium oxide-stabilized zirconium oxide blocks for the CAD/ CAM technology Product Number: 686194
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1888-2020·2020-05-13
Inpeco Centrifuge Module Recall for Potential Unbalanced Load Damage
Inpeco S.A. is recalling 23 Abbott Accelerator a3600 Centrifuge Modules because a loading algorithm defect may cause unbalanced loads that could damage the equipment.
Product
Abbott Accelerator a3600 Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions: CM_1-7-0.H86 or xCMd_2-5-0.elf and CM_1-7-1.H86 or xCMd_2-5-1-849fad9.elf
Category
Medical Device
Distribution
27 states
HighFDA (Devices)·Z-1864-2020·2020-05-13
Maquet Hemashield Vascular Grafts Recalled for Potential Seam Holes
Maquet is recalling Hemashield Platinum vascular grafts due to potential small holes at seam lines that could cause intra-operative bleeding.
Product
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00202175728AP0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1918-2020·2020-05-13
ICU Medical Recalls IV Administration Sets with Incorrect Drop Cannula
ICU Medical is recalling 25 units of IV administration sets that may contain a 15 drops/mL cannula instead of 10 drops/mL, risking under-delivery of critical medication.
Product
REF: Z2850, 112" (284 cm) 10 Drop Primary set w/2 Clave, Remv 3 Gang 1o2 Manifold w/3 Clave, Baseplate, Rotating Luer w/Filter Cap, 1 Ext, Sterile R, UDI: (01)00887709028241
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-1919-2020·2020-05-13
ICU Medical Recalls IV Administration Sets with Incorrect Drop Cannula
ICU Medical is recalling 275 units of IV administration sets that may contain a 15 drops/mL cannula instead of 10 drops/mL, risking under-delivery of critical medications.
Product
REF: Z3239, 126" 10 Drop Primary Set w/3 MicroClave, 2 Gang 4-Way Stopcocks, Rotating Luer, 1 Ext, Sterile R, UDI: (01)00887709030473
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-1905-2020·2020-05-13
Medtronic Recalls Visualase Cooled Laser Applicator System Tubing Sets
Medtronic is recalling Visualase Cooled Laser Applicator System tubing sets due to assembly defects that may disrupt saline flow.
Product
Visualase Cooled Laser Applicator System Tubing Set kits Product numbers: VCLAS 9735559, 3mm tip/1.65mm catheter VCLAS 9735560, 10mm tip/1.65mm catheter VCLAS 9735561, 15mm tip/1.85mm catheter
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1906-2020·2020-05-13
Intuitive Surgical Recalls da Vinci SP Instrument Arm Drapes
Intuitive Surgical is recalling da Vinci SP Instrument Arm Drapes because they may tear, compromising the sterile barrier.
Product
da Vinci SP Instrument Arm Drape. REF 430013-12 QTY 1 Pouch
Category
Medical Device
Distribution
17 states
ModerateFDA (Drugs)·D-1259-2020·2020-05-13
Sandoz Recalls Infuvite Pediatric Injection Due to Defective Container Crimping
Sandoz is recalling 17,500 units of Infuvite Pediatric Multiple Vitamins Injection due to sub-optimal crimping in the vial. The product was distributed nationwide.
Product
INFUVITE PEDIATRIC — INFUVITE PEDIATRIC (MULTIPLE VITAMINS INJECTION)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1856-2020·2020-05-13
Nobel Biocare Universal Base Abutments Recalled for Incorrect Screws
Nobel Biocare is recalling 238 Universal Base CC RP 1.5 mm abutments because they may contain incorrect screws that could loosen.
Product
Universal Base CC RP 1.5 mm; The Universal Base Abutment in combination with Nobel Biocare end osseous implants are indicated for single-unit if screw retained and for multiple-unit if cement retained crowns are used; catalog no. 38214 - Product Usage: Dental implant abutments…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1857-2020·2020-05-13
Nobel Biocare Recalls Dental Implant Abutments Due to Incorrect Screws
Nobel Biocare is recalling 478 Temporary Snap Abutments because packages may contain incorrect screws that could loosen, requiring retightening.
Product
Temporary Snap Abutment Engaging CC RP 1.5 mm; Pre-manufactured prosthetic components directly connected to the endosseous implant; catalog no. 38761 - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1853-2020·2020-05-13
Nobel Biocare Recalls Dental Implant Abutments Due to Incorrect Screw Risk
Nobel Biocare is recalling 239 units of Temporary Abutment Engaging CC RP components because packages may contain incorrect screws that could loosen.
Product
Temporary Abutment Engaging CC RP pre-manufactured prosthetic components directly connected to the endosseous implant, catalog no. 36664 - - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth replacements to…
Category
Medical Device
Distribution
Distributed nationwide