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Recalls affecting Utah

Data last updated: September 7, 2026 at 12:15 AM UTC

16,456 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 10, 2014

Naturalyte Liquid Bicarbonate Concentrate, 6.4 Liter Bottle Part Number: 08-4000-LB The concentrate is formulated to be used with a three steam hemodialysis machine which is calibrated for acid and bicarbonate concentrates

Naturalyte Liquid Bicarbonate maybe contaminated

ALL 50 STATES
Full report

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

Recall #:
67922
Lot/product code:
Lot Numbers (49 lots) recalled on 4/10/14: 13KMLB001 13LMLB001 14AMLB002 13KMLB002 13LMLB002 14AMLB003 13KMLB003 13LMLB003 14AMLB004 13KMLB004 13LMLB004 14AMLB005 13KMLB005 13LMLB005 14AMLB006 13KMLB006 13LMLB006 14AMLB007 13KMLB007 13LMLB007 14AMLB008 13KMLB008 13LMLB008 14AMLB009 13KMLB009 13LMLB009 14AMLB010 13KMLB010 13LMLB010 14AMLB012 13KMLB011 13LMLB011 13JMLB005 13KMLB012 13LMLB012 13JMLB008 13KMLB013 13LMLB013 13JMLB006 13KMLB014 13LMLB014 13JMLB007 13KMLB015 13LMLB015 13JMLB004 13KMLB016 13LMLB016 13KMLB017 14AMLB001 Expanded Recall (9 lots): 13LMLB005 13LMLB006 14AMLB011 14AMLB013 14AMLB014 14AMLB015 14AMLB016 14AMLB017 14BLMB001 Lorem ipsum dolor sit amet, consectetur adipiscing elit. Praesent at nibh ullamcorper, accumsan lectus at, tincidunt enim. Proin aliquet augue non dolor cursus, a luctus purus porttitor. Nulla facilisi. Nulla facilisi. Ut tincidunt eros ut fermentum iaculis. Vestibulum vel ornare tortor, id faucibus eros. Sed maximus quis sapien eu rhoncus. Proin pulvinar ipsum felis, at congue elit commodo tincidunt. Suspendisse lacus purus, convallis at velit ut, laoreet eleifend mauris.   Maecenas nisi enim, facilisis sed lorem eu, ultricies pellentesque mi. Curabitur accumsan vitae purus nec dictum. Sed efficitur rhoncus risus at cursus. In sollicitudin orci nec sem lobortis, ut posuere lacus porttitor. Nulla consequat diam metus, ut malesuada libero bibendum mattis. Aliquam porta augue vitae tellus euismod fermentum. Nulla in turpis vitae justo lacinia porttitor facilisis posuere ante. Praesent a egestas urna. Suspendisse laoreet condimentum risus sit amet molestie. Praesent fringilla augue eu risus gravida, nec rutrum tortor ultrices. Donec vitae feugiat leo. Nunc sit amet nisi erat. Maecenas tincidunt tristique diam, non venenatis urna egestas at.   Morbi ut tortor purus. Etiam eleifend dictum ultricies. Nullam convallis massa nec mi laoreet imperdiet. Interdum et malesuada fames ac ante ipsum primis in faucibus. Duis iaculis auctor vestibulum. Praesent rhoncus ligula bibendum elit luctus placerat. Aenean porta vehicula cursus. Morbi vitae ex eget tortor vehicula ultricies ut id augue. Donec sit amet orci dapibus, lacinia felis ut, ultricies erat. Aliquam ultricies risus in ligula viverra gravida. Mauris elementum, quam consectetur suscipit porta, odio eros ornare magna, eget imperdiet ligula nunc et metus. Cras sit amet turpis arcu. Ut feugiat lorem diam, sit amet vehicula quam ullamcorper nec.   Curabitur sed urna sed elit ultrices dapibus. Donec semper quam nec ligula volutpat porttitor. Donec non viverra nunc. Maecenas auctor purus quam, quis venenatis odio convallis quis. Morbi tempor congue libero, vitae tincidunt justo facilisis nec. Pellentesque placerat, urna quis rhoncus imperdiet, justo lorem faucibus dolor, vel consectetur urna nisi quis purus. Proin blandit justo eu convallis finibus.   Aenean tristique tempus mauris, non ullamcorper velit mollis at. Fusce sit amet ante lectus. Morbi nec tristique dolor, in placerat leo. Sed nulla sapien, commodo in magna sit amet, pharetra pharetra neque. Duis iaculis urna eget tellus laoreet finibus sit amet nec velit. Pellentesque pharetra sed elit at porttitor. Aliquam dapibus, augue et consequat facilisis, felis orci lacinia turpis, quis gravida sapien purus congue nisi. Duis condimentum arcu lobortis volutpat faucibus. Fusce velit ipsum, malesuada vitae facilisis non, molestie at tellus. Suspendisse auctor, elit vel suscipit mollis, felis erat tempus urna, eu bibendum felis mauris sit amet sem. Sed posuere purus vitae urna consequat placerat. Proin sed eros at odio pellentesque egestas. Nulla at luctus turpis. Quisque placerat, nisi dignissim commodo euismod, lacus diam sodales metus, a posuere ligula arcu nec quam.   Sed pharetra a velit a mattis. Suspendisse ullamcorper efficitur massa sed tempor. Vestibulum dapibus, diam a posuere pellentesque, neque est interdum metus, et scelerisque sapien nisl eget nibh. Fusce et leo ornare, aliquet augue eget, dignissim tellus. Nullam id elit et arcu fringilla lobortis quis non tellus. Morbi fringilla nec nunc sed rutrum. Curabitur nec nunc vel risus blandit porttitor vel sed risus. Integer nec luctus lectus, vel euismod sapien. Donec maximus egestas mi, quis hendrerit metus vestibulum at. Nunc nec ex lacinia nibh cursus semper consectetur quis eros. Donec nec lectus et erat fermentum luctus. Fusce lacinia neque et euismod pretium.   Morbi a dolor at libero tincidunt sagittis. Vestibulum sollicitudin urna est, eu tincidunt urna porttitor et. Quisque id magna sed nunc interdum ultrices id vel urna. Interdum et malesuada fames ac ante ipsum primis in faucibus. Fusce eu ligula iaculis, sodales libero at, tincidunt quam. Nunc egestas sagittis mauris, sit amet viverra lectus viverra id. In iaculis, mi id consequat tincidunt, risus nisi mattis odio, sit amet hendrerit dolor ipsum at eros. Sed rutrum, massa id semper congue, dolor lacus dignissim tortor, eu imperdiet justo dolor aliquet nibh. Nu… (truncated, 10712 characters total — see the official FDA record for the full value)
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 29, 2014

Saluta (reduced glutathione) Powder for Injection, 600 mg/vial, packaged in 10 vials per box, Exclusively Distributed by: QAF Pharmaceuticals Inc. Philippines, Unit Unit 202 ECG Building, Multinational Avenue, Multinational Village, Parahaque City, Metro Manila Philippines; Manufactured by: Shandong Luye Pharmaceutical Co. Ltd, Yantai Shandong, PRC la Luye Pharma Subsidiary, UPC 6920425209014

Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use as an antidote.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1318-2014
Lot/product code:
Lot #: 201302275, Exp 01/20/15; 201308384, Exp 10/19/2015
Recalling firm:
Flawless Beauty LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 29, 2014

Tatiomax (reduced glutathione/hydrolyzed collagen) powder for injection vials, 1200 mg/200 mg, 10-count vials per box, Manufactured by: Sujie Pharmaceutical Ltd., Tokyo, Japan, UPC 4973430081576

Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose labeling includes drug claims to act as an antidote.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1317-2014
Lot/product code:
Lot #: UB302, Exp 05/12/15
Recalling firm:
Flawless Beauty LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 29, 2014

Vitamin C (ascorbic acid) Injection, USP, 500 mg per 2 mL, 50 x 2 mL ampoules per box, Manufactured by: TP Drug Laboratories (1969) Co., Ltd., 98 Soi Sukhumvlt 62, Yak 1, Bangchak, Prakanong, Bangkok 10260, Thailand, Reg. No. 1 A 1557/30; UPC 8 853533 000533

Marketed Without An Approved NDA/ANDA: Parenteral product is sold over the counter whose labeling indicates it is to be used for the treatment of disease.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1320-2014
Lot/product code:
Lot #: 556273, Exp 9/25/16; 556219, Exp 8/2/16, or any other lot distributed by Flawless Beauty.
Recalling firm:
Flawless Beauty LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 29, 2014

Laroscorbine Platinium (vitamin C/collagen) injectable I.V. solution, 1 gm/0.35 gm, 5 mL ampoules, packaged in 10-count ampoules per box, Laboratories Roche Nicholas S.A., F-74240 Gaillard, - Tel.: 04 50 87 70 70, Fabricant : Produits Roche, 52, Bld du Parc, 92521 Neulilly -sur-Seine Cedex, barcode *3421357*

Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose labeling includes drug claims to act as an antidote.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1316-2014
Lot/product code:
Lot #: F040, Exp 08/16
Recalling firm:
Flawless Beauty LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 29, 2014

Sterile Water for Injection, 5 mL ampoules, packaged in 50-count ampoules per box, Manufactured and Distributed by: Euro Med Laboratories, UPC 4800573016219

Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose labeling indicates it is to be used for parenteral injection.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1321-2014
Lot/product code:
Lot #: 16U394, Exp 04/16; 16U421, Exp 08/16; 16U423, Exp 09/16
Recalling firm:
Flawless Beauty LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled April 29, 2014

Relumins Advanced Glutathione (lyophilized glutathione/vitamin C) injectable solution, 1500 mg/500 mg, packaged in 8-count vials, 8-count 5 mL vitamin C (ascorbic acid) solution diluent ampoules, and 30-count Advanced Glutathione Boosters capsules per box, Relumins Labs, 183 Locust Avenue, West Long Branch, NJ 07764, UPC 700175760302

Marketed Without An Approved NDA/ANDA: Product is sold over the counter whose labeling indicates it is to be used parenterally for drug claims.

ALL 50 STATES
Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1319-2014
Lot/product code:
Lot #: 130616, Exp 06/16
Recalling firm:
Flawless Beauty LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 26, 2014

Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e) REF 352952 : Reusable surgical knife handles, which are intended for use with blades which are inserted into a slot in the handle.

The knife handles slot depth is not meeting quality requirements, so blades may not fit on the handles properly.

ALL 50 STATES
Full report

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

Recall #:
78207
Lot/product code:
a) REF 352950: Lot numbers: D6, J6, E6, F6, G6, H6, I6 b) REF 352953: Lot numbers: I6, B6, E6  c) REF 352951: Lot numbers: I6, J6 d) REF 352957: Lot numbers: A6, B6, B7, K6, L6 e) REF 352952: Lot numbers: H6
Recalling firm:
Teleflex Medical
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 21, 2014

Hypodermic Needle Pro Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.

Needle is not captured in the needle safety sheath in specific lots.

ALL 50 STATES
Full report

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

Recall #:
69842
Lot/product code:
Lot Numbers: 2731779, 2763138, 2771516, 2771517
Recalling firm:
Smiths Medical ASD, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 21, 2014

Hypodermic Needle Pro Edge" Safety Device with Syringe 20G x1 5mL Luer lock syringe; Reorder Number: 452010 Product Usage: The Needle Pro Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.

Needle is not captured in the needle safety sheath in specific lots.

ALL 50 STATES
Full report

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

Recall #:
69842
Lot/product code:
Lot Number: 2755713
Recalling firm:
Smiths Medical ASD, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 21, 2014

Hypodermic Needle Pro Edge" Safety Device with Syringe 20G x1 10mL Luer lock syringe; Reorder Number: 4102010 Product Usage: The Needle Pro Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.

Needle is not captured in the needle safety sheath in specific lots.

ALL 50 STATES
Full report

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

Recall #:
69842
Lot/product code:
Lot Numbers: 2756526, 2771498
Recalling firm:
Smiths Medical ASD, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 22, 2015

MiniCap with Povidone-Iodine Solution, item number 5C4466P, for hemodialysis.

Product may have separating or protruding sponges

ALL 50 STATES
Full report

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

Recall #:
70512
Lot/product code:
Lot Numbers: GD896845, Exp. 10/2015; GD897371, Exp. 01/2016; GD896936, Exp. 10/2015; GD897124, Exp. 11/2015; GD897165, Exp. 12/2015; GD897157, Exp. 12/2015; GD896944, Exp. 11/2015; GD896837, Exp. 10/2015
Recalling firm:
Baxter Healthcare Corp.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Knee Arthro Pack and Knee Arthro Pack II - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 888-2359, 888-2531, 888-2351
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Arthroscopy Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 888-2605
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Bariatric Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 682-678
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Lima Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 682-927
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Face Neck Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 693-167
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Shoulder Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 888-2349
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Podiatry Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 888-2378, 888-2411, 888-2429, 888-2553
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Vaginal Rejuvenation Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 693-222
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Orthopedic Split Drape Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 888-2604
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Suction Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 670-057
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Abdominal Pack and Abdom Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 670-056, 681-014
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Tummy Tuck Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 693-223
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 20, 2015

Gyn Pack - contains Devon Light Glove Used during surgery

Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.

ALL 50 STATES
Full report

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

Recall #:
71130
Lot/product code:
Pack 693-111
Recalling firm:
Stradis Healthcare, LLC.
View official FDA record (opens in a new tab)