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Recalls affecting Massachusetts

Data last updated: September 8, 2026 at 1:13 PM UTC

17,003 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/virusAnnounced 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/virusAnnounced 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)
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)
UnclassifiedAllergenUndeclaredAnnounced 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)
UnclassifiedBacteria/virusAnnounced 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/virusAnnounced 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 April 25, 2019

Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed above a dynamic indoor flume designed for modeling water erosion in an indoor research environment with limited human access

Failure to comply event due to incorrect labeling of a class 1 laser product.

ALL 50 STATES
Full report

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

Recall #:
83302
Lot/product code:
Model: L1, identified by Accession No. RH19A0069
Recalling firm:
ASTRA, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject 201 Vet Pak Hypodermic Needle, 18 ga x 1-1/2 Item code: 8881201548

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 904219, 904220, 907710
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject 201 Vet Pak Hypodermic Needle, 20 ga x 1-1/2" Item code: 8881201498

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 905611
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 27 G x 1-1/4" Item code: 8881200508

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 904901
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 18 G x 1-1/2" Item code: 8881200078

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 907007
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 14 G x 1-1/2" Item code: 8881200011

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 904218, 904918, 906329
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 20 G x 1-1/2" bulk Item code: 8881200664

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 905657, 906327, 906341
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject 201 Vet Pak Hypodermic Needle, 22 ga x 1-1/2" Item code: 8881201456

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 909117
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code: 8881200037

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number:904212, 905612, 907002
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject 201 Vet Pak Hypodermic Needle, 19 ga x 1-1/2 Item code: 8881201522

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 905662
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code:8881200045

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 905613
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Standard Hypodermic Needle Item code: 8881200029

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 904956
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Blunt Cannula, 22 G x 1-1/2" (0.711 mm x 3.8 cm) Item code: 8881202389

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 903530
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 902108
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Blunt Cannula, 16 G x 1-1/2" (1.651 mm x 3.8 cm) Item code: 8881202322

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 902110, 902111
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Blunt Cannula, 20 G x 1-1/2" (0.902 mm x 3.8 cm) Item code: 8881202363

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 907734
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Blunt Cannula, 15 G x 1-1/2" (1.829 mm x 3.8 cm) Item code: 8881202314

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 905659, 905660, 906343
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 30, 2019

Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355

Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product

ALL 50 STATES
Full report

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

Recall #:
82927
Lot/product code:
Lot Number: 905617, 905618, 905619, 905620, 907004, 907005
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 3, 2019

Monarch Medical Technologies EndoTool IV, Versions 1.8, Version 1.8.5 and higher, and Version 1.9 and Version 1.10.

Insulin dosing calculations were erroneously high.

ALL 50 STATES
Full report

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

Recall #:
82828
Lot/product code:
Versions 1.8, Version 1.8.5 and higher, and Version 1.9 and Version 1.10
Recalling firm:
Monarch Medical Technologies
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 9, 2019

Rim Plate, 10-Hole, Left, PRS RX System. Titanium, implantable - Product Usage: The implant temporarily stabilizes bone segments until bony consolidation has taken place. After this, the implant has no more use and can be removed.

The titanium implant has the wrong article number laser marked on it.

ALL 50 STATES
Full report

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

Recall #:
82796
Lot/product code:
Model Number: 21206-10; Lot Code: 26/F42778
Recalling firm:
I.T.S. GmbH
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 15, 2019

InterStim(TM) System, Model Numbers: a) TH90G01 b) TH90GFA c) TH90G02 d) TH90G03 Product Usage: The Medtronic Model A510 Clinician application (app) is intended for use with the HH90 Handset and TM90 Communicator to program, adjust, and troubleshoot the Medtronic Models 3023 and 3058 InterStim neurostimulators for sacral neuromodulation therapy. The clinician uses the Clinician app to program settings for the patient. The A510 Clinician app, HH90 Handset, TM90 Communicator along with the A520 Patient app are only sold as a kit (TH90).

There is a potential for an unexpected increase in stimulation during InterStim programming with the A10 Clinician Application (on Medtronic's smart programmer).

ALL 50 STATES
Full report

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

Recall #:
82626
Lot/product code:
Model Numbers/UDI: a) TH90G01/00763000058005  b) TH90GFA/00763000187231 c) TH90G02/00763000192259, 00763000192266, 00763000192273,  00763000192280, 00763000192297, 00763000192303, 00763000192310 d) TH90G03/00763000192310  ALL LOT/SERIAL NUMBERS
Recalling firm:
Medtronic Neuromodulation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 17, 2019

EGIA 60 CURVED TIP ART MED THICK SULU, EGIA60CTAMT

The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.

ALL 50 STATES
Full report

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

Recall #:
82950
Lot/product code:
N8L0311KY N8M0063KY
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 17, 2019

EGIA 45 ARTICULATING MED THICK SULU, Item Code EGIA45AMT

The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.

ALL 50 STATES
Full report

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

Recall #:
82950
Lot/product code:
lots N4D0328KX N4D0338KX N4E0796KX N4E0846KX N4E0980KX N4E1018KX N4E1059KX N4E1173KX N4E1269KX N4E1654KX N4E1655KX N4G0523KX N4G1541KX N4H0078KX N4J0215KX N4J0250KX N4J0271KX N4J1002KX N4J1217KX N4J1247KX N4K1465KX N4M0921KX N5B0285KX N5B0340KX N5B0417KX N5B0484KX N5B0680KX N5D0467KX N5D0497KX N5D0550KX N5D0609KX N5D0660KX N5D0736KX N5D0765KX N5D1008KX N5E0068KX N5E0143KX N5E0297KX N5E0727KX N5E0756KX N5F0096KX N5F1223KX N5F1382KX N5G0244KX N5G0329KX N5G0339KX N5G0355KX N5G0405KX N5G0414KX N5G0809KX N5G0868KX N5J1153KX N5J1201KX N5J1233KX N5K0045KX N5K0089KX N5K0115KX N5M0172KX N5M0662KX N5M0693KX N5M0732KX N5M0741KX N6A0913KX N6B0332KX N6C0462KX N6D0388KX N6D0474KX N6D0506KX N6E0078KX N6E0099KX N6E0117KX N6E0129KX N6E0366KX N6E0416KX N6F0039KX N6F0088KX N6F0156KX N6F0720KX N6F0780KX N6F0816KX N6G0099KX N6G0139KX N6G0191KX N6G0198KX N6G0213KX N6G0243KX N6G0280KX N6H0168KX N6H0247KX N6H0291KX N6H0327KX N6H0370KX N6H0433KX N6H0456KX N6H0466KX N6H0792KX N6H0827KX N6J0152KX N6J0185KX N6J0243KX N6J0476KX N6K0160KX N6K0209KX N6K0251KX N6K0293KX N6K0676KX N6K0739KX N6K0774KX N6K0824KX N6K0871KX N6K1137KX N6L0806KX N6L0814KRX N6L0909KX N6L0942KX N6L0944KX N6M0065KX N6M0095KX N6M0113KX N6M0134KX N6M0263KX N7A0293KX N7A0792KX N7B0070KX N7B0125KX N7B0154KX N7B0177KX N7B0885KX N7B0905KX N7B0946KX N7C0387KX N7C0405KX N7C0442KX N7C0485KX N7C0517KX N7C0775KX N7C0812KX N7C0857KX N7C0899KX N7C0927KX N7C0977KX N7C1014KX N7D0101KX N7D0135KX N7D0182KX N7D0226KX N7D0247KX N7D0264KX N7D0416KX N7D0473KX N7D0495KX N7D0538KX N7D0591KX N7D0918KX N7D0945KX N7E0372KX N7E0518KX N7E0565KX N7E0610KX N7E0920KX N7E0962KX N7F0093KX N7F0094KX N7F0186KX N7F0224KX N7F0662KX N7F0663KX N7F0696KX N7F0745KX N7F0822KX N7F1019KX N7F1052KX N7F1139KX N7G0016KX N7G0241KX N7G0279KX N7G0498KX N7G0790KX N7G0904KX N7H0012KX N7H0174KX N7H0315KX N7H0347KX N7H0419KX N7H0470KX N7H0520KX N7H0569KX N7H0712KX N7H0786KX N7H0957KX N7H1017KX N7H1057KX N7H1096KX N7H1141KX N7H1175KX N7H1187KX N7J0070KX N7J0099KX N7J0135KX N7J0174KX N7J0483KX N7J0508KX N7J0550KX N7J0636KX N7J0692KX N7J0858KX N7J0897KX N7J1014KX N7J1155KX N7K0008KX N7K0085KX N7K0087KX N7K0154KX N7K0225KX N7K0270KX N7K0272KX N7K0303KX N7K0307KX N7K0400KX N7K0443KX N7K0500KX N7K0544KX N7K0562KX N7K0711KX N7K0742KX N7K0783KX N7K0821KX N7K0904KX N7K0956KX N7K1052KX N7K1150KX N7K1181KX N7K1183KX N7L0057KX N7L0091KX N7L0132KX N7L0361KX N7L0403KX N7L0431KX N7L0475KX N7L0592KX N7L0811KX N7L0856KX N7L1004KX N7L1098KX N7M0100KX N7M0132KX N7M0506KX N7M0554KX N7M0589KX N7M0592KX N7M0614KX N7M0620KX N7M0778KX N7M0918KX N7M0967KX N7M1000KX N8A0065KX N8A0203KX N8A0380KX N8A0381KX N8A0772KX N8A0960KX N8A1028KX N8A1050KX N8A1099KX N8A1119KX N8B0114KX N8B0137KX N8B0204KX N8B0571KX N8B0641KX N8B0666KX N8B0709KX N8B0769KX N8B0805KX N8B0849KX N8B0885KX N8B0905KX N8B0958KX N8B1009KX N8B1034KX N8B1048KX N8C0159KX N8C0324KX N8C0340KX N8C0470KX N8C0546KX N8C0589KX N8C0718KX N8C0777KX N8C0779KX N8C0816KX N8C1338KX N8C1339KX N8D0043KX N8D0083KX N8D0142KX N8D0311KX N8D0312KX N8D0394KX N8D0482KX N8D0483KX N8D0536KX N8D0594KX N8D0647KX N8D0694KX N8D1045KX N8D1067KX N8E0081KX N8E0149KX N8E0201KX N8E0233KX N8E0266KX N8E0321KX N8E0378KX N8E0431KX N8E0435KX N8E0498KX N8E0567KX N8E0612KX N8E0659KX N8E0699KX N8E0700KX N8E0725KX N8F0094KX N8F0183KX N8F0258KX N8F0307KX N8F0335KX N8F0347KX N8F0383KX N8F0428KX N8F0482KX N8F0658KX N8F0691KX N8F0773KX N8F0858KX N8F0879KX N8F0921KX N8F0976KX N8F1015KX N8F1046KX N8G0871KX N8G0911KX N8G0942KX N8G0980KX N8H0683KX N8H0735KX N8H0759KX N8J0819KX N8L0895KY N8M0168KRY N9A0665KRY N9A0954KRY N9B0348KY
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 17, 2019

EGIA 30 ARTICULATING MED THICK SULU, Item Code EGIA30AMT

The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.

ALL 50 STATES
Full report

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

Recall #:
82950
Lot/product code:
lots N5A0871KX N7A0527KX N7E0441KX N8J0039KX N8J0527KX N8J0820KX
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 17, 2019

EGIA 60 ARTICULATING EXTRA THICK SULU, Item code EGIA60AXT

The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.

ALL 50 STATES
Full report

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

Recall #:
82950
Lot/product code:
N6B0079KX N8A0029KX
Recalling firm:
Covidien LLC
View official FDA record (opens in a new tab)