State

Alabama product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41926–41950 of 80187

SevereFDA (Devices)·Z-1824-2018·2018-05-23
Medtronic Recalls Endo GIA Stapler Kits Due to Missing Sled Component
Medtronic is recalling 171,271 Endo GIA stapler kits worldwide because a missing sled component may prevent staple formation, leading to bleeding or leakage.
Product
Covidien" Best Practices" Procedure Kits containing Auto Suture" Endo GIA" Devices Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1814-2018·2018-05-23
Medtronic Recalls Endo GIA Stapler Loading Units Due to Missing Sled Component
Medtronic is recalling 171,271 Endo GIA Auto Suture Universal Articulating Loading Units because a missing sled component may prevent staple formation, risking bleeding or leakage.
Product
Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm- 2.0mm ( Item Code 030450) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1847-2018·2018-05-23
Medtronic Endo GIA Universal Staplers Recalled for Missing Sled Component
Medtronic is recalling 169,775 Endo GIA Universal and Universal XL staplers worldwide and in the US because a missing sled component may prevent staple formation, risking bleeding or leakage.
Product
(1) BOX LAPZD ZESTAW DO SG (2) BOX LAPISG1 ZESTAW DO SG (3) BOX LAPISGW ZESTAW DO SG Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1843-2018·2018-05-23
Medtronic Recalls Bariatric Surgical Kits Due to Missing Staple Sled Component
Medtronic is recalling 169,775 bariatric surgical kits worldwide because a missing sled component may prevent staple formation, risking bleeding or leakage.
Product
(1)LAPBARLECZNA ZESTAW BARIATRYCZNY LECZNA (2) KITBAR021- BARIATRIC KIT X1 Item Code:KITBAR021- BARIATRIC KIT X0 (3)BOX SGGLOGX1 ZESTAW DO BARIATRII Item Code: SGGLOGX1 ZESTAW DO BARIATRII (4)BOX SGGLOGX1 ZESTAW DO BARIATRII Item Coder:SGGLOGX1 ZESTAW DO…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1454-2018·2018-05-23
eBars Recalls Organic Dark Cocoa Raspberry Bars for Peanut Allergen
eBars is recalling 26,180 units of TRIM Organic Dark Cocoa Raspberry bars because they tested positive for peanut, an allergen not declared on the label.
Product
TRIM ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.8 OZ (51g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00423 1
Category
Food
Distribution
40 states
SevereFDA (Devices)·Z-1840-2018·2018-05-23
Medtronic Endo GIA Universal Staplers Recalled for Missing Sled Component
Medtronic is recalling Endo GIA Universal and Universal XL staplers because a missing sled component may prevent staple formation, leading to bleeding or leakage.
Product
(1) BOX KITDE0143 BYPASS BOX (Item Number: KITDE0143, KITDE0143 BYPASS BOX) (2) BOX KITDE0154 BYPASS KH NORDWEST (Item Number: KITDE0154, KITDE0154 BYPASS KH NORDWEST Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1865-2018·2018-05-23
Medtronic Endo GIA Staplers Recalled for Missing Sled Component
Medtronic is recalling Endo GIA staplers because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
BOX VMIN ZESTAW DO VATS PODSTAWOWY Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1452-2018·2018-05-23
eBars Recalls Organic Dark Cocoa Raspberry Bars for Undeclared Peanut Allergen
eBars is recalling 2,903 units of RUN Organic Dark Cocoa Raspberry bars because testing revealed the presence of peanut, an allergen not declared on the product label.
Product
RUN ORGANIC DARK COCOA RASPBERRY bar NET WT. 1.6 OZ (45g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00412 7
Category
Food
Distribution
40 states
SevereFDA (Devices)·Z-1825-2018·2018-05-23
Medtronic Endo GIA Universal Staplers Recalled for Missing Sled Component
Medtronic is recalling Endo GIA Universal staplers because a missing sled component may prevent staple formation, leading to bleeding or leakage.
Product
BOX KIT1095V KIT OBESITAS (Item Code KIT1095V) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1821-2018·2018-05-23
Medtronic Recalls Endo GIA Stapler Reloads Due to Missing Sled Component
Medtronic is recalling 171,271 Endo GIA 30mm stapler reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
Endo GIA" 30mm Gray Curved Tip Articulating Vascular Reload with Tri-Staple" Technology( Item Code EGIA30CTAV) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1447-2018·2018-05-23
eBars Recalls Organic Chocolate Almond Bars Due to Peanut Allergen
eBars is recalling GOLF Organic Chocolate Almonds bars because they tested positive for peanut, an undeclared allergen. The recall covers 5,391 bags distributed across 37 states.
Product
GOLF ORGANIC CHOCOLATE ALMONDS bar NET WT. 1.6 OZ (45g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00400 4
Category
Food
Distribution
40 states
SevereFDA (Devices)·Z-1859-2018·2018-05-23
Medtronic Endo GIA Stapler Sleeves Recalled for Missing Sled Component
Medtronic is recalling 169,775 Endo GIA stapler sleeves worldwide due to a missing sled component that may prevent staple formation, risking bleeding or leakage.
Product
(1)BOX SLEEVEGK3 (2) BOX SLEEVEGK4 SLEEVE GASTRECTOMY (3)BOX SLEEVEJAWI SLEEVE GASTRECTOMY BOX (4) SSLEEVE ZEST DO SLEEVE GASTREKTOMIIX1 Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1817-2018·2018-05-23
Medtronic Endo GIA Stapler Loading Units Recalled for Missing Sled Component
Medtronic is recalling 171,271 Endo GIA Auto Suture Universal Articulating Loading Units because a missing sled component may prevent staple formation, risking bleeding or leakage.
Product
Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm - 2.5mm( Item Code 030454) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1828-2018·2018-05-23
Medtronic Endo GIA Universal Staplers Recalled for Missing Sled Component
Medtronic is recalling 171,271 Endo GIA Universal staplers because a missing sled component may prevent staple formation, risking bleeding or leakage.
Product
BOX1073076GASB1 BBR GASTRIC BYPASS S(Item Code BOX1073076GASB1 BBR GASTRIC BYPASS S) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1866-2018·2018-05-23
Medtronic Endo GIA Staplers Recalled for Missing Sled Component
Medtronic is recalling Endo GIA universal staplers because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
BOX VWR ZESTAW DO VATS KLIN Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is determined by…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1820-2018·2018-05-23
Medtronic Recalls Endo GIA Stapler Loading Units Due to Missing Sled
Medtronic is recalling 171,271 Endo GIA Auto Suture Universal Articulating Loading Units because a missing sled component may prevent staple formation, leading to bleeding or leakage.
Product
Endo GIA" Auto Suture" Universal Articulating Loading Unit 60mm - 3.5mm ( Item Code 030458) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1822-2018·2018-05-23
Medtronic Endo GIA Stapler Reloads Recalled for Missing Sled Component
Medtronic is recalling Endo GIA 30mm stapler reloads because a missing sled component may cause staple failure, leading to bleeding or leakage.
Product
Endo GIA" 30mm Gray Curved Tip Articulating Vascular Reload with Tri-Staple" Technology( Item Code EGIA30AV) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1444-2018·2018-05-23
eBars Recalls Organic Peanut Butter Bars for Undeclared Almonds
eBars is recalling FIT Organic Peanut Butter Chocolate Raspberry bars because they contain undeclared almonds. The recall was initiated after notification from the State of Tennessee.
Product
FIT ORGANIC PEANUT BUTTER CHOCOLATE RASPBERRY bar NET WT 1.8 OZ (51g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00443 1
Category
Food
Distribution
40 states
SevereFDA (Devices)·Z-1837-2018·2018-05-23
Medtronic Endo GIA Universal Bypass Kits Recalled for Missing Sled Component
Medtronic is recalling specific Endo GIA Universal Bypass Kits because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
KIT-DE-0080 BYPASS KIT LOHNE X1( Item KIT-DE-0080) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1849-2018·2018-05-23
Medtronic Recalls Bariatric Staplers Due to Missing Sled Component
Medtronic is recalling specific bariatric stapler kits because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
(1)BOX PST01199 BARIATRIC TRISTAPLE (Item Number: PST01199) (2) BOX PST03403 ALTERNATIVE APPENDIX KIT (Item Number: PST03403) (3) BOX PST03533 KIT APP STAPLER (Item Number: PST03403) Product Usage: The Endo GIA universal and…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1832-2018·2018-05-23
COVIDIEN Medtronic Recalls Endo GIA Stapler Kits Due to Missing Sled
COVIDIEN Medtronic is recalling Endo GIA universal stapler kits because a missing sled component may prevent proper staple deployment, risking bleeding or leakage.
Product
BOX KIT00713 KIT BY PASS Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is determined by the…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1451-2018·2018-05-23
eBars Recalls Run Organic Chocolate Almond Bars for Peanut Allergen
eBars is recalling Run Organic Chocolate Almond bars because they tested positive for peanut, an allergen not declared on the label.
Product
RUN ORGANIC CHOCOLATE ALMOND bar NET WT. 1.6 OZ (45g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00404 2
Category
Food
Distribution
40 states
SevereFDA (Food)·F-1450-2018·2018-05-23
eBars Recalls Organic Chocolate Almond Bars Due to Peanut Allergen
eBars is recalling 48,969 units of MAN Organic Chocolate Almond bars because they tested positive for peanut, an undeclared allergen.
Product
MAN ORGANIC CHOCOLATE ALMOND bar NET WT. 1.8 OZ (51g) Manufactured and Distributed by eBars, LLC, Franklin, TN 37064 UPC 8 55529 00414 1
Category
Food
Distribution
40 states
SevereFDA (Drugs)·D-0840-2018·2018-05-23
Apotex Recalls Subpotent Piperacillin and Tazobactam Injection Vials
Apotex Inc. is recalling specific lots of Piperacillin and Tazobactam for Injection due to high impurity levels that decreased the drug's potency.
Product
Piperacillin and Tazobactam for Injection, USP 4.5 gram/vial* 10-count Single Use Vials per carton, Rx only, Mfg. by: Hospira Healthcare India Pvt. Ltd. Irungattukottai-602 105, India Mfg. for: Apotex Corp. Weston, FL 33326. NDC 60505-0688-4
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1839-2018·2018-05-23
Medtronic Recalls Bypass Kits Due to Missing Stapler Component
Medtronic is recalling 171,271 Endo GIA Bypass Kits because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
BOX KITDE0108 BYPASS KIT LUEBECK ( KITDE0108) Product Usage: The Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples…
Category
Medical Device
Distribution
Distributed nationwide