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Recalls affecting Nebraska

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

16,502 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 IHigh risk
FoodForeign materialRecalled September 24, 2019

Chef Pierre ¿ SMALL WHOLE GRAIN BANANA MUFFINS NET WT 12 LB (5.44kg) 4 TRAYS/24/2 oz WHOLE GRAIN BANANA MUFFINS KEEP FROZEN CONTAINS WHEAT, EGGS DISTRIBUTED BY TYSON FOOD SERVICE SPRINGDALE, AR 72765-2020 UPC (01) 1 00 32100 08896 8

The firm was notified from a consumer of foreign material in the product. After examination they discovered that the foreign material was "tree nut".

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0040-2020
Lot/product code:
Product: 08896 CP SMMUF 2OZ WG BNNA 4/24CT Lot Codes: 1700072910:15,1700072910:16, 1700072910:17, 1700072910:18, 1700072910:19, 1700072910:20, 1700072910:21, 1700072910:22, 1700072910:23 & 1700072910:00 expiration 3/12/2020
Recalling firm:
Sara Lee Frozen Bakery
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 24, 2019

MOSAIQ, oncology information system - Product Usage: MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery.

The user may inadvertently enter Metric values into Height and Weight fields labeled with US Standard Units.

ALL 50 STATES
Full report

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

Recall #:
85240
Lot/product code:
Software Versions (UDI/GTIN): MOSAIQ 2.00 (00858164002305); MOSAIQ 2.20 (00858164002312); MOSAIQ 2.30 (00858164002329); MOSAIQ 2.40 (00858164002077); MOSAIQ 2.41 (00858164002084); MOSAIQ 2.60 -2.64 (00858164002091); MOSAIQ 2.50 (00858164002107); MOSAIQ 2.65 (00858164002220); MOSAIQ 2.70 (00858164002037); MOSAIQ 2.80 (00858164002251); MOSAIQ 2.81 (00858164002282)
Recalling firm:
Elekta Impac Software
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled September 24, 2019

Walgreens Regular Strength Wal-Zan 75 Ranitidine Tablets, USP 75 mg/Acid Reducer 30 Tablets NDC 0363-1029-03 Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015

GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).

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-0315-2020
Lot/product code:
All lots remaining within expiry.
Recalling firm:
Apotex Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled September 24, 2019

Rite Aid Pharmacy Maximum Strength Ranitidine Tablets, USP 150 mg-acid reducer Distributed By: Rite Aid 30 Hunter Lane Camp Hill, PA 17011 a) 50 tablets NDC 11822-6052-1; b) 65 tablets NDC 11822-6052-2; c) 95 tablets NDC 11822-4727-3; d) 24 tablets NDC 11822-6051-8

GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).

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-0319-2020
Lot/product code:
All lots remaining within expiry.
Recalling firm:
Apotex Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled September 24, 2019

Walgreens Maximum Strength Wal-Zan 150 Ranitidine Tablets, USP 150 mg/Acid Reducer Distributed By: Walgreen Co., 200 Wilmot RD., Deerfield, IL 60015 a) 200 Tablets NDC 0363-1030-07; b) 24 Tablets NDC 0363-1030-02; c) 95 Tablets NDC 0363-1030-09; d) 65 Tablets NDC 0363-1030-06

GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (NDMA).

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-0314-2020
Lot/product code:
All lots remaining within expiry.
Recalling firm:
Apotex Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled September 27, 2019

EQ-400-RH-QZ and EQ-400-LH-BK products Product Usage: The device is a very broadband light source emitting incoherent non-laser light from the Deep UV through the visible wavelengths.

On September 27, 2019 Energetiq Technology (the manufacturer) discovered a problem with their EQ-400-RH-QZ and EQ-400-LH-BK products during routine manufacturing functional testing. It was noted that a safety interlock within the lamp does not function in a reliable manner to shut down the system if the laser collimator is removed from the lamp while the system is operating. This is a potential safety hazard for anyone working on or nearby the lamp.

ALL 50 STATES
Full report

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

Recall #:
84378
Lot/product code:
The defect concerns a total of fifteen (15) of our EQ-400 products. manufactured between June 3, 2016 and September 26, 2019.
Recalling firm:
Energetiq Technology Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 75 mg, a.) 30- count bottles (NDC 0363-0131-30), b.) 80-count bottles (NDC 0363-0131-80) (Walgreens) OTC

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0183-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Dr. Reddy's Ranitidine Tablets, USP 150 mg, 24 count bottles, NDC 55111-404-34 (OTC)

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0182-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets 75 mg, a.) 30 count bottles (NDC 63868-482-30), 60 count bottles (NDC 63868-482-60) (CDMA) OTC

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0175-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 150 mg, a.) 65 count bottles (NDC 49035-404-61) b.) 130 count bottles (NDC 49035-404-13) c.) 220 count bottles (NDC 49035-404-65) (Walmart) OTC

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0171-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 150 mg, a.) 24 count bottles (NDC 0363-0010-34), b.) 65 count bottles (NDC 0363-0010-61) , c.) 95 count bottles (NDC 0363-0010-62), d.) 200 count bottles (NDC 0363-0010-01) (Walgreens) OTC

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0170-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Dr. Reddy's: Ranitidine Capsules 150 mg, Rx a.) 60 count bottles (NDC 55111-129-60) b.) 500 count bottles (NDC 55111-129-05)

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0168-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 150 mg, a.) 24 count bottles (NDC 63868-480-24), b.) 50-count bottles (NDC 63868-480-50) (CDMA) OTC

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0184-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 150 mg, 190 count bottles (2x95) Tray (Sam's Club) OTC, NDC 150062076 UPC Code 078742089720

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0169-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 75 mg 30 count bottles (NDC 30142-131-30) (Kroger)

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0174-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 75 mg, NDC 57896-715 (GeriCare) OTC.

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0178-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Dr. Reddy's Ranitidine Tablets, USP 75 mg, 60 count bottles, NDC 55111-131-60, (OTC)

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0181-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 150 mg, a.) 24 count bottles (NDC 30142-505-34), b.) 50 count bottles (NDC 30142-505-50) (Kroger) OTC

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0172-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 150 mg, NDC 57896-717 (GeriCare) OTC

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0185-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Dr. Reddy's Ranitidine Capsules, USP 300 mg, a.) 30 count bottles (NDC 55111-130-30) b.) 100 count bottles (NDC 55111-130-01)

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0180-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 150 mg, a.) 24 count bottles (NDC 71713-203-02), b.)95 count bottles (NDC 71713-203-05) (Thirty Madison) OTC.

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0177-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 75 mg, a.) 30 count bottles (NDC 69842-871-30) b.) 80 count bottles (NDC 69842-871-80) c.)160 count bottles (NDC 69842-871-37) (CVS) OTC

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0173-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 150 mg, a.) 95 count bottles (NDC 43598-808-62), b.) 220 count bottles (NDC 43598-808-65) (HCA) OTC.

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0176-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled October 1, 2019

Ranitidine Tablets, USP 150 mg, 40 count bottles, NDC 11673-849-40 (Target) OTC.

CGMP Deviations: Presence of NDMA impurity detected in product.

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-0179-2020
Lot/product code:
Batch Numbers: All lots within expiry.
Recalling firm:
Dr. Reddy's Laboratories, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 3, 2019

Programmers & Remote Monitoring Software Apps: 2090 CareLink Programmer

There is a potential for Medtronic programmer and remote monitoring software applications to display an inaccurate remaining longevity estimate for a subset of implanted cardiac device models. This issue does not impact device functionality.

ALL 50 STATES
Full report

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

Recall #:
84026
Lot/product code:
Serial Numbers:  PKK051331R PKK200187R PKK209956R PKK207572R PKK209265R PKK016592R PKK202460R PKK019811R PKK209256R PKK007753R PKK015981R PKK016604R PKK017955R PKK018301R PKK019555R PKK019776R PKK051452R PKK052792R PKK204491R PKK204504R PKK204551R PKK204575R PKK204595R PKK204640R PKK204740R PKK203409R PKK006360R PKK202461R PKK018408R PKK019864R PKK204483R PKK016046R PKK016047R PKK019820R PKK020201R PKK010563R PKK209937R PKK209928R PKK050581R PKK209305R PKK211241R PKK209294R PKK201567R PKK206687R PKK211282R PKK208961R PKK209373R PKK202996R PKK210858R PKK202566R PKK211233R PKK205628R PKK209203R PKK211710R PKK100124R PKK211042R PKK210807R PKK200224R PKK208864R PKK209197R PKK208958R PKK209332R PKK211720R PKK016352R PKK019371R PKK211286R PKK202507R PKK205997R PKK205974R PKK202465R PKK017835R PKK018895R PKK201637R PKK201640R PKK201643R PKK201645R PKK202394R PKK202397R PKK202411R PKK202428R PKK202441R PKK202444R PKK202451R PKK202454R PKK202459R PKK202463R PKK202464R PKK202466R PKK202489R PKK202494R PKK202521R PKK202550R PKK202552R PKK202553R PKK202557R PKK202558R PKK202561R PKK202563R PKK202564R PKK202565R PKK202567R PKK204964R PKK204973R PKK204974R PKK204983R PKK204985R PKK205962R PKK205968R PKK205970R PKK205977R PKK205979R PKK205982R PKK205986R PKK205989R PKK205994R PKK205998R PKK205999R PKK206000R PKK207397R PKK207399R PKK207576R PKK207588R PKK207601R PKK207603R PKK207604R PKK207606R PKK207607R PKK207615R PKK207621R PKK207622R PKK207623R PKK207628R PKK207649R PKK207650R PKK208500R PKK208503R PKK208508R PKK208510R PKK211023R PKK211064R PKK211072R PKK211084R PKK211100R PKK211227R PKK211228R PKK211229R PKK211235R PKK211238R PKK211239R PKK211284R PKK211289R PKK211294R PKK211339R PKK211342R PKK203579R PKK107297R PKK108724R PKK108726R PKK108729R PKK109569R PKK201389R PKK201402R PKK051032R PKK051031R PKK010204R PKK106139R PKK106149R PKK106153R PKK106161R PKK106164R PKK106212R PKK106221R PKK106224R PKK106228R PKK054839R PKK054899R PKK054903R PKK006109R PKK011161R PKK011162R PKK012402R PKK012404R PKK020167R PKK052616R PKK052619R PKK208773R PKK206171R PKK108840R PKK205827R PKK018974R PKK054297R PKK052590R PKK055474R PKK019344R PKK208281R PKK020200R PKK056378R PKK107503R PKK106539R PKK005940R PKK201926R PKK202805R PKK205627R PKK003769R PKK016555R PKK004307R PKK001417R PKK006119R PKK005232R PKK004040R PKK013386R PKK019411R PKK052102R PKK018098R PKK101253R PKK205556R PKK102674R PKK006689R PKK200245R PKK106865R PKK211492R PKK017878R PKK010764R PKK211518R PKK211521R PKK057197R PKK011242R PKK200949R PKK051450R PKK018218R PKK057195R PKK201686R PKK020573R PKK014310R PKK054238R PKK209424R PKK208646R PKK208224R PKK020366R PKK207934R PKK053799R PKK108035R PKK204464R PKK051548R PKK203435R PKK014418R PKK102204R PKK050960R PKK108305R PKK001172R PKK102818R PKK205393R PKK013868R PKK053717R PKK053233R PKK002545R PKK202693R PKK002871R PKK106723R PKK055305R PKK108322R PKK102503R PKK202024R PKK003498R PKK004347R PKK015584R PKK105180R PKK003235R PKK014949R PKK018886R PKK019330R PKK104774R PKK014465R PKK054834R PKK055373R PKK101011R PKK106795R PKK205887R PKK205332R PKK002384R PKK015619R PKK055620R PKK003926R PKK006407R PKK007261R PKK014428R PKK017571R PKK019868R PKK050318R PKK107143R PKK006589R PKK018884R PKK103154R PKK107158R PKK204136R PKK015641R PKK104118R PKK001847R PKK002178R PKK053006R PKK017686R PKK211216R PKK201780R PKK015586R PKK101918R PKK006674R PKK013504R PKK052353R PKK100694R PKK102490R PKK106404R PKK003165R PKK007298R PKK052052R PKK105856R PKK100708R PKK052050R PKK102715R PKK006557R PKK101957R PKK002398R PKK004434R PKK006460R PKK101141R PKK003318R PKK017784R PKK107927R PKK209592R PKK052937R PKK103113R PKK103401R PKK107979R PKK102706R PKK103417R PKK051039R PKK108929R PKK002518R PKK018602R PKK014370R PKK050450R PKK018051R PKK018954R PKK006683R PKK015308R PKK206137R PKK017096R PKK201696R PKK013110R PKK053602R PKK103395R PKK104573R PKK106395R PKK106663R PKK107105R PKK108835R PKK019743R PKK002029R PKK006880R PKK007419R PKK052069R PKK012323R PKK051108R PKK207988R PKK053982R PKK055228R PKK201744R PKK002557R PKK208342R PKK013078R PKK014144R PKK014900R PKK055981R PKK103121R PKK001953R PKK005823R PKK007818R PKK005994R PKK015611R PKK051055R PKK056120R PKK056431R PKK014363R PKK014324R PKK017674R PKK019498R PKK003199R PKK005355R PKK007162R PKK103381R PKK013092R PKK056024R PKK056434R PKK103151R PKK104749R PKK106810R PKK107817R PKK010011R PKK206429R PKK004752R PKK003279R PKK011923R PKK208647R PKK004440R PKK208616R PKK202512R PKK208696R PKK002498R PKK208692R PKK101219R PKK006587R PKK018978R PKK055097R PKK207723R PKK106912R PKK203509R PKK201788R PKK006737R PKK206152R PKK011005R PKK015511R PKK012410R PKK015570R PKK019464R PKK013598R PKK001597R PKK007512R PKK018480R PKK100995R PKK003991R PKK004471R PKK105584R PKK001580R PKK011440R PKK053484R PKK002364R PKK010024R PKK050689R PKK006639R PKK014435R PKK011200R PKK205410R PKK055049R PKK102825R PKK104021R PKK014983R PKK017725R PKK050719R PKK005068R PKK107473R PKK017915R PKK104060R PKK208481R PKK107727R … (truncated, 501142 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
View official FDA record (opens in a new tab)