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Recalls affecting Wisconsin

Data last updated: September 9, 2026 at 1:18 PM UTC

16,927 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Mendietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced September 4, 2026

Foods AliveMoringa Leaf Powder

Potential to be contaminated with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusE. coliAnnounced September 3, 2026

Great ValueOrganic Triple Berry Blend

Possible E. Coli Contamination

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc.Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenMilkUndeclaredAnnounced August 31, 2026

Little TemptationsChocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

LipofitLipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

KofinasGarlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaE. coliAnnounced August 29, 2026

Everything SproutsRobust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced August 29, 2026

MartinaMangoes

Potential contamination with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
Wording
UnclassifiedRisk not yet known
Medical deviceRecalled November 18, 2020

IceRod" i-Thaw" Prostate Cryoablation Kit

Complaint trend regarding needle shaft gas leaks.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86777
Lot/product code:
UPN: FPRPR4070  UDIs: 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830105, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830075, 7290104830099, 7290104830099, 7290104830099, 7290104830099, 7290104830099, 7290104830105  Batch Numbers: U1363, U0865, U0555, U0542, U0151, U0150, U0054, U0053, U0046, U0037, U0036, T0633, T0515, T0430, T0274, T0273, T0201, T0188, T0167, A7174, A7100, A7044, A7022, A7021, A6788, A6740, A2117, A2019, A1968, A1753, A1605, A1535, A1430, A1429, A1235, U1262, U1114, U1036, U0910, U0909, U0863, U0365, U0280, U0281, U0180, U0088, U0038, T0529, T0457, T0235, T0178, T0058, A6911, A6835, A6695, A6648, A2133, A2040, A2033, A1889, A1634, A1368, A1225, G5063, G5871, G5900, G5902, G5975, P1901
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 18, 2020

IceFORCE" 2.1 CX L 90 Cryoablation Needle

Complaint trend regarding needle shaft gas leaks.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86777
Lot/product code:
UPN: FPRPR3618  UDIs: 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089, 7290104831089  Batch Numbers: U1214, U1215, U1112, U1113, U0958, U0959, U0861, U0862, U0765, U0766, U0729, U0730, U0645, U0643, U0644, U0642, U0426, U0425, U0408, U0160, U0161, T0278, T0275, T0143, T0142, T0134, T0135, A7082, A7032, A7033, A6677, A6678, A2030, A2029, A1775, A1774, A1658, A1544, A1545, A1526, A1188, A1189
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 18, 2020

IceSphere" 1.5 90 Cryoablation Needle

Complaint trend regarding needle shaft gas leaks.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86777
Lot/product code:
UPN: FPRPR3560  UDIs: 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945  Batch Numbers: U1454, U1455, U1456, U1420, U1421, U1325, U1326, U1328, U1327, U0435, U0432, U0369, U0351, U0352, T0403, T0402, T0395, T0394, T0305, T0146, T0126, T0006, T0023, T0024, T0018, T0015, A7205, A6966, A6967, A6969, A6968, A6943, A6942, A6917, A6918, A2089, A2090, A1858, A1857, A1848, A1847, A1823, A1824, A1819, A1818, A1811, A1812, A1801, A1802, A1794, A1793, A1785, A1786, A1601, A1602, A1591, A1592, A1489, A1490, A1477, A1478, A1309, A1308, A1294, A1295, A1293, A1292, A1265, A1264, A1250, A1251, A1242, A1241
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 19, 2020

Medtronic HVAD Pump Implant Kits, labeled as: a. PUMP 1103, b. PUMP 1104, c. PUMP 1104JP, d. PUMP 1100, e. Model 1101, f. Model 1102, g. Model 1104CA-CLIN, h. Model 1205, i. Model MCS1705PU

Pumps manufactured with impellers from a subset of lots from a single supplier are failing to initially start, restart, or experiencing a delay in restart within the maximum number of restart attempts at a rate substantially higher than pump in the overall population.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86924
Lot/product code:
a. Model Number 1103: GTIN 00888707003261, Serial Numbers HW40002, HW40004, HW40006, HW40009, HW40017, HW40025, HW40045, HW40046, HW40048, HW40049, HW40051, HW40054, HW40061, HW40067, HW40068, HW40073, HW40074, HW40075, HW40079, HW40085, HW40087, HW40089, HW40090, HW40094, HW40097, HW40099, HW40100, HW40109, HW40112, HW40120, HW40121, HW40122, HW40138, HW40139, HW40143, HW40145, HW40147, HW40149, HW40152, HW40153, HW40154, HW40157, HW40166, HW40168, HW40169, HW40176, HW40177, HW40178, HW40186, HW40189, HW40190, HW40192, HW40197, HW40199, HW40200, HW40201, HW40202, HW40206, HW40209, HW40210, HW40211, HW40212, HW40223, HW40226, HW40230, HW40232, HW40238, HW40240, HW40245, HW40247, HW40259, HW40262, HW40263, HW40270, HW40271, HW40272, HW40273, HW40281, HW40283, HW40288, HW40292, HW40293, HW40294, HW40295, HW40298, HW40299, HW40301, HW40302, HW40303, HW40305, HW40307, HW40317, HW40322, HW40324, HW40326, HW40329, HW40334, HW40337, HW40340, HW40359, HW40371, HW40373, HW40376, HW40381, HW40384, HW40390, HW40392, HW40395, HW40397, HW40399, HW40402, HW40405, HW40433, HW40436, HW40440, HW40443, HW40444, HW40445, HW40448, HW40453, HW40455, HW40460, HW40466, HW40481, HW40482, HW40483, HW40488, HW40489, HW40490, HW40491, HW40499, HW40501, HW40503, HW40504, HW40509, HW40510, HW40512, HW40515, HW40517, HW40518, HW40520, HW40523, HW40524, HW40527, HW40528, HW40529, HW40530, HW40533, HW40534, HW40537, HW40546, HW40558, HW40567, HW40568, HW40569, HW40572, HW40576, HW40583, HW40585, HW40590, HW40592, HW40593, HW40595, HW40605, HW40606, HW40616, HW40620, HW40621, HW40622, HW40627, HW40631, HW40633, HW40635, HW40636, HW40644, HW40672, HW40678, HW40682, HW40683, HW40684, HW40687, HW40690, HW40694, HW40696, HW40700, HW40703, HW40705, HW40708, HW40710, HW40715, HW40717, HW40718, HW40719, HW40723, HW40728, HW40732, HW40737, HW40739, HW40744, HW40745, HW40746, HW40749, HW40750, HW40753, HW40755, HW40757, HW40759, HW40762, HW40766, HW40767, HW40769, HW40772, HW40776, HW40778, HW40780, HW40783, HW40800, HW40801, HW40805, HW40807, HW40810, HW40813, HW40815, HW40819, HW40821, HW40829, HW40831, HW40832, HW40834, HW40838, HW40841, HW40857, HW40861, HW40862, HW40863, HW40865, HW40868, HW40870, HW40874, HW40875, HW40876, HW40882, HW40883, HW40884, HW40891, HW40894, HW40902, HW40903, HW40905, HW40908, HW40913, HW40916, HW40917, HW40918, HW40922, HW40924, HW40925, HW40927, HW40928, HW40930, HW40935, HW40939, HW40941, HW40944, HW40948, HW40962, HW40967, HW40968, HW40976, HW40977, HW40986, HW40987, HW40988, HW40991, HW40995, HW40998, HW41001, HW41005, HW41007, HW41008, HW41012, HW41017, HW41022, HW41032, HW41035, HW41038, HW41054, HW41057, HW41058, HW41059, HW41060, HW41064, HW41066, HW41069, HW41072, HW41073, HW41076, HW41077, HW41081, HW41084, HW41092, HW41097, HW41098, HW41100, HW41104, HW41105, HW41107, HW41111, HW41115, HW41124, HW41131, HW41137, HW41138, HW41146, HW41148, HW41154, HW41157, HW41158, HW41165, HW41167, HW41172, HW41176, HW41179, HW41180, HW41182, HW41185, HW41186, HW41188, HW41194, HW41195, HW41207, HW41208, HW41225, HW41227, HW41228, HW41229, HW41232, HW41234, HW41237, HW41238, HW41240, HW41247, HW41248, HW41250, HW41275, HW41276, HW41278, HW41280, HW41283, HW41288, HW41289, HW41291, HW41295, HW41298, HW41300, HW41310, HW41318, HW41321, HW41327, HW41330, HW41331, HW41334, HW41338, HW41341, HW41345, HW41351, HW41360, HW41361, HW41381, HW41382, HW41385, HW41388, HW41389, HW41393, HW41394, HW41400, HW41404, HW41410, HW41412, HW41419, HW41421, HW41423, HW41424, HW41425, HW41427, HW41431, HW41432, HW41435, HW41438, HW41441, HW41443, HW41444, HW41451, HW41453, HW41456, HW41457, HW41459, HW41461, HW41463, HW41464, HW41468, HW41470, HW41478, HW41479, HW41480, HW41481, HW41489, HW41492, HW41497, HW41503, HW41504, HW41508, HW41509, HW41517, HW41519, HW41524, HW41525, HW41529, HW41531, HW41537, HW41548, HW41551, HW41556, HW41573, HW41577, HW41578, HW41584, HW41585, HW41586, HW41588, HW41589, HW41590, HW41591, HW41594, HW41596, HW41598, HW41603, HW41605, HW41608, HW41614, HW41616, HW41618, HW41626, HW41627, HW41630, HW41631, HW41636, HW41642, HW41650, HW41657, HW41659, HW41662, HW41664, HW41666, HW41668, HW41678, HW41679, HW41681, HW41688, HW41692, HW41702, HW41703, HW41707, HW41708, HW41712, HW41719, HW41729, HW41731, HW41733, HW41735, HW41747, HW41748, HW41749, HW41756, HW41772, HW41787, HW41795, HW41797, HW41807, HW41812, HW41814, HW41816, HW41820, HW41821, HW41822, HW41823, HW41836, HW41841, HW41844, HW41861, HW41866, HW41867, HW41873, HW41880, HW42121, HW42125, HW42129, HW42134, HW42142, HW42144, HW42210, HW42220, HW42242, HW42260, HW42277, HW42279, HW42281, HW42283, HW42323, HW42324, HW42343, HW42389, HW42727, HW42736, HW42768, HW42804, HW42810, HW42819, HW42770. GTIN 00888707002639, Serial Numbers: HW29766, HW29809, HW29831, HW29874, HW29946, HW30015, HW31099, HW31169, HW31174, HW31177, HW31181, HW31189, HW31215, HW31246, HW31278, HW31279, HW31281, HW31289, HW31302, HW31313, HW31347, HW31349, HW31361, HW31363, HW31369, HW3138… (truncated, 177937 characters total — see the official FDA record for the full value)
Recalling firm:
Heartware, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 20, 2020

Haag Streit Surgical Floor stands FS 2-11 (Ref no. 615H511) and FS 2-15 (Ref no. 615H515) in combination with the operating microscopes HS Hi-R NEO 900 (Ref no. 657 820) and HS Hi-R NEO 900A (Ref no. 657 821), with software REF 615 588 versions 2.0 to 3.3 - Product Usage: use in ophthalmology and in other disciplines with vertical direction of view

Software error -Software REF 615 588 versions 2.0 to 3.3, movement of the focusing is triggered by pressing the button of the footswitch it might occur that the movement does not stop when releasing the button, result in potential risk to the patient's eye

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86707
Lot/product code:
Floor stands FS 2-11, FS 2-15 with the software REF 615 588 in versions 2.0 to 3.3.   FS 2-11 Ref. # 615H511 Serial Numbers:From 1001; FS 2-15 Ref. #615H515 Serial Numbers From 1001; HS Hi-R NEO 900 Ref. # 657 Serial Numbers 820 from 101; HS Hi-R NEO 900A Ref # 657 821 Serial Numbers from 101   Unique Device Identifier (UDI)  HS Hi-R NEO 900 +EMWM657 820 0/$+serial no.  HS Hi-R NEO 900A +EMWM657 821 0/$+serial no.  FS 2 11 +EMWM 615H5110/$+serial no.  FS 2-15 +EMWM 615H515 0/$+serial no.
Recalling firm:
Haag-Streit USA Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Naturalyte Liquid Acid concentrate drums, Product Code 13-2251-0 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously communicated. Calcium concentration is below manufacturing specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86939
Lot/product code:
Lot Numbers: 20LXAC025 20LXAC081 20LXAC082 20LXAC083  Additional Affected lots as of 3/17/21: 20LXAC029 20NXAC021 20LXAC026 20LXAC065 20LXAC028 20NXAC029 20LXAC071 20LXAC103 20LXAC027 20LXAC070 20LXAC067 20NXAC019 20LXAC082 20LXAC025 20LXAC081 20LXAC083
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Citrasate Liquid Acid concentrate drums, Product Code 13-2251 -CA - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously communicated. Calcium concentration is below manufacturing specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86939
Lot/product code:
Lot Numbers: 20LXAC033 20NXAC004  Additional Affected lots as of 3/17/21: 20LXAC031 20NXAC004 20LXAC033 20NXAC003 20LXAC032
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Naturalyte Liquid Acid concentrate bottles, Product Code 08-3251-9 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously communicated. Calcium concentration is below manufacturing specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86939
Lot/product code:
Lot Numbers: 20LXAC058 20LXAC078 20LXAC096 20NXAC011 20NXAC012  Additional Affected lots as of 3/17/21: 20LXAC060 20NXAC026 20LXAC045 20LXAC043 20LXAC078 20NXAC012 20LXAC058 20LXAC096 20NXAC011 20LXAC059 20LXAC044 20LXAC079
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Naturalyte Liquid Acid concentrate bottles, Product Code 08-2251-0 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously communicated. Calcium concentration is below manufacturing specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86939
Lot/product code:
Lot Numbers: 20LXAC076 20LXAC077 20LXAC091 20LXAC101 20NXAC010  Additional Affected lots as of 3/17/21: 20LXAC053 20LXAC047 20LXAC054 20LXAC049 20NXAC016 20LXAC094 20NXAC024 20NXAC025 20LXAC091 20LXAC101 20LXAC077 20LXAC048 20NXAC010 20LXAC076
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Covidien TA Auto Suture Vascular Loading Unit with DST Series Technology 30 mm- V3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or transection of tissue. Item Number: TA30V3L

May contain a damaged internal component which could impede staple deployment and result in incomplete staple formation and a non-functional staple line preventing adequate hemostasis, or leading to anastomotic leak, pneumothorax, tissue damage or other delayed secondary complications including infection, peritonitis, and sepsis

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86886
Lot/product code:
Lot Numbers: P0B1335MY, P0D0170MY, P0D1445M, 0F0377MY, P0B1336MY,P0D1444MY, P0E1211MY, P0F0606MY.  UDI: 10884521043152, 20884521043159
Recalling firm:
Covidien Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Naturalyte Liquid Acid concentrate bottles, Product Code 08-4231-0 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously communicated. Calcium concentration is below manufacturing specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86939
Lot/product code:
Lot Numbers: 20LXAC088  Additional Affected lots as of 3/17/21: 20LXAC088 20LXAC052
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Naturalyte Liquid Acid concentrate drums, Product Code 13-3251-9 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously communicated. Calcium concentration is below manufacturing specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86939
Lot/product code:
Lot Numbers: 20LXAC066 20LXAC089  Additional Affected lots as of 3/17/21: 20LXAC066 20LXAC073 20LXAC074 20LXAC024 20LXAC023 20LXAC072 20LXAC085 20LXAC089
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

ADVIA Gamma-Glutamyl Transferase (GGT) Reagent - Product Usage: For in vitro diagnostic use in the quantitative determination of gamma-glutamyl transferase in human serum and plasma. Siemens Material Number (SMN): ADVIA Chemistry: 10309495 (20 mL) 10316298 (70 mL)

Gamma-Glutamyl Transferase (GGT) Reagent Low End Repeatability-Imprecision. Reagent may demonstrate a coefficient of variation (%CV) outside of the performance data for repeatability (within-run) listed in the Instructions For Use (IFU) on some analyzers.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86900
Lot/product code:
All lot codes. UDI: 10309495 (20 mL) = 00630414508344 10316298 (70 mL) = 00630414209753
Recalling firm:
Siemens Healthcare Diagnostics, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6) - Product Usage: intended to be used for the controlled administration of fluids.

There is a potential software error during programming.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86758
Lot/product code:
Product Code 35700ABB, GTIN 00085412091570
Recalling firm:
Baxter Healthcare Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Covidien TA Auto Suture Vascular Stapler with DST Series Technology 30mm-V 3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or transection of tissue. Item Number: TA30V3S

May contain a damaged internal component which could impede staple deployment and result in incomplete staple formation and a non-functional staple line preventing adequate hemostasis, or leading to anastomotic leak, pneumothorax, tissue damage or other delayed secondary complications including infection, peritonitis, and sepsis

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86886
Lot/product code:
Lot Numbers: P0B1142MY, P0C1515MY, P0E0634MY, P0E1353MY, P0C0492MY,P0D1454MYP0E1352MY,P0G0601Y, P0C0493MY  UDI: 10884521043145, 20884521043142
Recalling firm:
Covidien Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Atellica Gamma-Glutamyl Transferase (GGT) Reagent - Product Usage: For in vitro diagnostic use in the quantitative determination of gamma-glutamyl transferase in human serum and plasma. Siemens Material Number (SMN): 11097597

Gamma-Glutamyl Transferase (GGT) Reagent Low End Repeatability-Imprecision. Reagent may demonstrate a coefficient of variation (%CV) outside of the performance data for repeatability (within-run) listed in the Instructions For Use (IFU) on some analyzers.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86900
Lot/product code:
All lot codes. UDI: 00630414596440
Recalling firm:
Siemens Healthcare Diagnostics, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6) - Product Usage: intended to be used for the controlled administration of fluids.

There is a potential software error during programming.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86758
Lot/product code:
Product Code 35700BAX, GTIN 00085412091587
Recalling firm:
Baxter Healthcare Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8) - Product Usage: intended to be used for the controlled administration of fluids.

There is a potential software error during programming.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86758
Lot/product code:
Product Code 35700BAX2, GTIN 00085412498683
Recalling firm:
Baxter Healthcare Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Naturalyte Liquid Acid concentrate bottles, Product Code 08-2301-3 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously communicated. Calcium concentration is below manufacturing specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86939
Lot/product code:
Lot Numbers: 20NXAC013 20NXAC035  Additional Affected lots as of 3/17/21: 20LXAC056 20LXAC041 20LXAC055 20LXAC057 20NXAC013 20NXAC035
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Citrasate Liquid Acid concentrate bottles, Product Code 08-2251-CA - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously communicated. Calcium concentration is below manufacturing specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86939
Lot/product code:
Lot Numbers: 20NXAC007  Additional Affected lots as of 3/17/21: 20NXAC007
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Naturalyte Liquid Acid concentrate bottles, Product Code 08-2201-5 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously communicated. Calcium concentration is below manufacturing specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86939
Lot/product code:
Lot Numbers: 20LXAC086 20LXAC099 20NXAC014  Additional Affected lots as of 3/17/21: 20LXAC061 20LXAC062 20LXAC099 20LXAC086 20NXAC014
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Baxter Spectrum IQ Infusion System with Dose IQ Safety Software - Product Usage: intended to be used for the controlled administration of fluids.

There is a potential software error during programming.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86758
Lot/product code:
Product Code 3570009, GTIN 00085412610900
Recalling firm:
Baxter Healthcare Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Naturalyte Liquid Acid concentrate bottles, Product Code 08-1251-1 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously communicated. Calcium concentration is below manufacturing specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86939
Lot/product code:
Lot Numbers: 20LXAC063 20NXAC008  Additional Affected lots as of 3/17/21: 20NXAC005 20LXAC098 20NXAC039 20NXAC008 20LXAC063
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

Naturalyte Liquid Acid concentrate bottles, Product Code 08-2351-8 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.

The deviation in conductivity for sodium level exceeds 0.6mS/cm from the theoretical conductivity (TCD) or approximately 6mEq/L of sodium from prescriptions that was previously communicated. Calcium concentration is below manufacturing specification.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
86939
Lot/product code:
Lot Numbers: 20NXAC033  Additional Affected lots as of 3/17/21: 20LXAC097 20NXAC033
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 30, 2020

Artis zee/ zeego & Artis Q/ Q.zen Artis Pheno

When the user changes frame rates from lower frequency (e.g. 10 f/s) to higher frequency (e.g. 30 f/s) during continuous release of Fluoro "Fluoro Override", the measured Air Kerma Rate can exceed the regulatory limits.

ALL 50 STATES
Full report

FDA has not published a risk classification for this recall yet.

Recall #:
87026
Lot/product code:
Model number: Artis zee floor- 10094135 Artis zee ceiling- 10094137 Artis zee multi-purpose- 10094139 Artis zee biplane- 10094141 Artis zeego- 10280959 Artis Pheno- 10849000 Artis Q floor- 10848280 Artis Q ceiling- 10848281 Artis Q biplane- 10848282 Artis Q zeego- 10848283 Artis Q.zen floor- 10848353 Artis Q.zen ceiling- 10848354 Artis Q.zen biplane- 10848355
Recalling firm:
Siemens Medical Solutions USA, Inc
View official FDA record (opens in a new tab)