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Recalls affecting Louisiana

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

16,895 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
Class IIModerate risk
DrugRecalled July 2, 2019

Walgreens Sodium Chloride Ophthalmic Solution, 5% Hypertonicity Eye Drops, 0.5 oz (15 mL), Distributed by : Walgreen Co 200 Wilmot Road Deerfield IL 60015 NDC 0363-0193-13

Not guaranteed to be germ-free

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-0362-2020
Lot/product code:
Lot #: 19105, Exp 04/22; 19050, Exp 02/22
Recalling firm:
Altaire Pharmaceuticals, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 2, 2019

CVS Health Lubricating Gel Drops for Anytime Use, Item#: 563420, Product Size: 10 mL, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895

Not guaranteed to be germ-free

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-0456-2020
Lot/product code:
17238 08/19 18094 4/20 19058 02/21
Recalling firm:
Altaire Pharmaceuticals, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 2, 2019

CVS Health Preservative Free Lubricant Eye Drops Fast Acting, Item#: 258625 Product Size: 0.6 mL x 60 ct, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895

Not guaranteed to be germ-free

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-0406-2020
Lot/product code:
RHD 08/19 RIF 09/19 RIN 09/19 RKP 11/19 SAR 01/20 SCG 03/20 SED 5/20
Recalling firm:
Altaire Pharmaceuticals, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 2, 2019

Walgreens Sodium Chloride Ophthalmic Ointment, 5% Hypertonicity Eye Ointment Sterile, Net Wt. 0.125 oz (3.5 g), Distributed by Walgreen Co. 200 Wilmot Road Deerfield, IL 60015, NDC 0363-7500-50

Not guaranteed to be germ-free

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-0361-2020
Lot/product code:
Lot #: TCI , Exp 03/21
Recalling firm:
Altaire Pharmaceuticals, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 2, 2019

OCuSOFT Eye Wash Sterile Isotonic Buffered Solution, 1 FL OZ (30 mL), Manufactured for OCuSOFT, Inc. Richmond, TX 77406-0429, NDC 54799-565-01

Not guaranteed to be germ-free

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-0447-2020
Lot/product code:
18026 1/21 18100 4/21 19052 2/22 19130 5/22
Recalling firm:
Altaire Pharmaceuticals, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled July 2, 2019

OCuSOFT Eye Wash Sterile Isotonic, 4 FL OZ (118 mL), Manufactured for OCuSOFT, INC Richmond, TX 7406-0429 Mfd. By: Altaire Pharmaceuticals, Inc. Aquebogue, NY 11931 Made in USA, NDC 54799-565-59

Not guaranteed to be germ-free

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-0448-2020
Lot/product code:
16268 10/19 11/07/2016 16301 11/19 12/09/2016 17088 3/20 4/28/2017 17109 4/20 6/14/2017 17318 10/20 11/10/2017 17323 10/20 1/12/2018 18014 1/21 2/21/2018 18045 2/21 3/16/2018 18059 3/21 5/25/2018 18063 3/21 18117 5/21 18134 5/2
Recalling firm:
Altaire Pharmaceuticals, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 3, 2019

Monaco RTP System, software versions 5.10 and 5.11, Radiation Treatment Planning System

When creating 3D plans using either MU or Dose weighting modes, if the user changes the number of fractions, rescales the plan and then changes the wedge angle, the Monitor Units are scaled incorrectly.

ALL 50 STATES
Full report

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

Recall #:
83273
Lot/product code:
all Monaco Radiation Treatment Planning units installed with software version 5.10 or 5.11
Recalling firm:
Elekta Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

NATURE'S OWN BUTTER HAMBURGER BUNS 8CT, UPC 72250 02313 9

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1602-2019
Lot/product code:
Lot#111, Best By Date July 18 2019
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

L'OVEN FRESH 8CT KAISER BUNS UPC 41498 11722 1

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1606-2019
Lot/product code:
Lot #111, Best By Date July 17 2019
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

Flowers Bratwurst Buns 12 CT UPC 7 22500 40792

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1597-2019
Lot/product code:
Lot #111 Best By Date July 18, 2019
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

Hot Dog Buns sold under the brand names of: CLOVER VALLEY 8CT UPC 70210 00760 1; FAMILY STYLE 8CT UPC 70210 01297 1; FLOWERS RESTAURANT 12CT UPC 70210 00640 6, UPC 70210 00649 9 & UPC 70210 00964 3; FOOD DEPOT 8CT UPC 72250 02439 6; GREAT VALUE 8CT UPC 78742 09728 2; IDEAL 8CT UPC 72250 02463 1; IGA 8CT UPC 41270 04244 4; LAURA LYNN 8CT UPC 86854 00784 6; MARLET PANTRY 8 CT UPC 85239 70133 1; NATURAL GRAIN 12CT UPC 73105 92059 7; OVEN FRESH 8CT UPC 72250 02438 9; PIGGLY WIGGLY 8CT UPC 41290 01313 4; PUBLIX 8CT UPC 41415 30790 2; SE GROCERS 8CT UPC 38259 10183 4; SUNBEAM 8CT UPC 77633 06374 0 & WONDER 8CT UPC 72250 02108 1

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1605-2019
Lot/product code:
CLOVER VALLEY, FAMILY STYLE, GREAT VALUE, IGA, MARLET PANTRY, OVEN FRESH, PIGGLY WIGGLY, PUBLIX, SE GROCERS & WONDER - Lot #111 & 180 Best By Date July 19 2019 FLOWERS RESTAURANT & NATURAL GRAIN - Lot #111 Best By Date July 18 2019 FOOD DEPOT, IDEAL, LAURA LYNN & SUNBEAM - Lot #180 Best By Date July 19 2019
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

WONDER HONEY HAMBURGER BUNS 8CT, UPC 72250 02112 8

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1603-2019
Lot/product code:
Lot#111, Best By Date July 18 2019
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

BBQ Bread & Pull-A-Part BBQ Bread sold under the brand names of Flowers UPC 7 22500 40792, Ingles UPC 8 68540 15348 & Wonder UPC 7 22500 20923

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1596-2019
Lot/product code:
FLOWERS BBQ BREAD - Lot# 180 Best By Date July 18, 2019: Ingles - Lot #180 Best By Date July 18, 2019 & Wonder - Lot #180 Best By Date July 18, 2019
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

Flowers Enriched Rolls UPC 70210 00686 4

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1600-2019
Lot/product code:
Lot #180 Best By Date July 18, 2019
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

100% Whole Wheat Hamburger Buns sold under the brand names of: FLOWERS 8CT No UPC; GREAT VALUE UPC 78742 00800 4 & NATURES OWN 8CT UPC 72250 00398 8

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1604-2019
Lot/product code:
All have the lot code - Lot#111, Best By Date July 18 2019
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

Dinner Rolls sold under the brand names of Laura Lynn UPC 86854 06669 0 & Wonder 12 CT UPC 72250 07421 6 24 CT UPC 72250 01169 3

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1599-2019
Lot/product code:
Laura Lynn Lot #180 Best By Date July 18, 2019; Wonder 12 & 24 CT - Lot #180 Best By Date July 18, 2019
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

Publix 12 CT Brown & Serve Rolls 12 CT UPC 41415 31190 9

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1598-2019
Lot/product code:
Lot #111 Best By Date July 18, 2019
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

Krystal 24 Sheet Sandwich Slider Buns

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1607-2019
Lot/product code:
Best By Date A JUL 11 07/06
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodRecalled July 9, 2019

Hamburger Buns soled under the brand names of: 7-ELEVEN 8CT, UPC 52548 00660 0; BRAVO 8CT, UPC 33755 85868 8; CBC NATHANS 8CT, UPC 72250 09366 8; CLOVER VALLEY 8CT, UPC 70210 00759 5; FAMILY STYLE 8CT, UPC 72250 02473 0; FOOD DEPOT 8CT, UPC 72250 02440 2; GREAT VALUE 8CT, UPC 78742 22375 9; GRISSOM'S MILL 8CT, UPC 51933 26740 4; HITCHCOCK'S 8CT, UPC 70210 10337 2; HOME PRIDE 16CT, UPC 72250 00658 3; IDEAL 8CT, UPC 72250 02507 2; IGA 8CT, UPC 41270 02548 5; LAURA LYNN 8CT, UPC 86854 00780 8; MARKET PANTRY 8CT, UPC 85239 03163 6; MEMBERS MARK 8CT/3 PK, UPC 93968 01393 6; NATURAL GRAIN 8CT, UPC 73105 92058 0; OVEN FRESH 8CT, UPC 72250 02471 6; PIGGLY WIGGLY 8CT, UPC 41290 01317 2; PUBLIX 8CT, UPC 41415 30690 5; SE GROCERS 8CT, UPC 38259 10182 7; SEDANO'S 8CT, UPC 72250 00031 4; SUNBEAM 8CT, UPC 77633 06328 3; WM 8CT HAMBURGER BUNS (PAN PARA SANDWICH), UPC 78742 04868 0 & WONDER 8CT, UPC 72250 02109 8.

The products have the potential to contain small pieces of hard plastic introduced during production process.

Full report

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

Recall #:
F-1601-2019
Lot/product code:
IGA 8CT, Lot #111 & Lot #180, Best By Date July 19 2019 7-ELEVEN 8CT, BRAVO 8CT, CBC NATHANS 8CT, GRISSOM'S MILL 8CT, HITCHCOCK'S 8CT, HOME PRIDE 16CT, MEMBERS MARK 8CT/3 PK, NATURAL GRAIN 8CT, PIGGLY WIGGLY 8CT, SEDANO'S 8CT, WM 8CT HAMBURGER BUNS (PAN PARA SANDWICH) & WONDER 8CT - Lot #111, Best By Date July 18 2019; CLOVER VALLEY 8CT, FAMILY STYLE 8CT, MARKET PANTRY 8CT, OVEN FRESH 8CT, PUBLIX 8CT & SE GROCERS 8CT, Lot #111, Best By Date July 18, 2019 and Lot #180, Best By Date July 19 2019 FOOD DEPOT 8CT, GREAT VALUE 8CT, IDEAL 8CT, LAURA LYNN 8CT & SUNBEAM 8CT, Lot #180, Best By Date July 19 2019
Recalling firm:
FLOWERS FOODS
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 10, 2019

ClubMax Laser Projection Series

The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could unintentionally expose the user and/or observers to high power laser radiation. It needs to be replaced for safety reasons.

ALL 50 STATES
Full report

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

Recall #:
83438
Lot/product code:
ClubMax Laser Projection Series
Recalling firm:
Gk Photonics Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 10, 2019

Atom Laser Projection Series

The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could unintentionally expose the user and/or observers to high power laser radiation. It needs to be replaced for safety reasons.

ALL 50 STATES
Full report

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

Recall #:
83438
Lot/product code:
Atom Laser Projection Series
Recalling firm:
Gk Photonics Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 10, 2019

Spectrum Laser Projection Series

The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could unintentionally expose the user and/or observers to high power laser radiation. It needs to be replaced for safety reasons.

ALL 50 STATES
Full report

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

Recall #:
83438
Lot/product code:
Spectrum Laser Projection Series
Recalling firm:
Gk Photonics Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 10, 2019

Maxim Laser Projection Series

The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could unintentionally expose the user and/or observers to high power laser radiation. It needs to be replaced for safety reasons.

ALL 50 STATES
Full report

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

Recall #:
83438
Lot/product code:
Maxim Laser Projection Series
Recalling firm:
Gk Photonics Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 10, 2019

Logolas Laser Projection Series

The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could unintentionally expose the user and/or observers to high power laser radiation. It needs to be replaced for safety reasons.

ALL 50 STATES
Full report

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

Recall #:
83438
Lot/product code:
Logolas Laser Projection Series
Recalling firm:
Gk Photonics Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled July 10, 2019

Burstberry Laser Projection Series

The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could unintentionally expose the user and/or observers to high power laser radiation. It needs to be replaced for safety reasons.

ALL 50 STATES
Full report

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

Recall #:
83438
Lot/product code:
Burstberry
Recalling firm:
Gk Photonics Inc
View official FDA record (opens in a new tab)