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Recalls affecting Ohio

Data last updated: September 10, 2026 at 1:16 PM UTC

17,192 recalls found

Just announced

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

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

Products contain undeclared yohimbine

Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

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

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

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

Foods AliveMoringa Leaf Powder

Potential to be contaminated with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

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

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

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

Presence of particulate matter identified as iron oxide

Full report
Drugs

Recalling firm: B. Braun Medical Inc.

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

Company contact: recalls@bbraunusa.com

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

Great ValueOrganic Triple Berry Blend

Possible E. Coli Contamination

Full report
Food & BeveragesFoodborne Illness

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

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

Company contact: Info.foodsafety@comfrut.com

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

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

Presence of particulate matter and lack of sterility assurance

Full report
Food & Beverages

Recalling firm: American Regent, Inc.

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

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

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

Undeclared milk

Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

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

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

LipofitLipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

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

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

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

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

Contains garlic essential oil not approved for culinary use

Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

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

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

Everything SproutsRobust Radish Mix, 5oz Cups

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

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

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

Company contact: everythingsproutsmn@gmail.com

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

MartinaMangoes

Potential contamination with Salmonella

Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

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

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
Wording
UnclassifiedRisk not yet known
Medical deviceRecalled November 23, 2020

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

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

ALL 50 STATES
Full report

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

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

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

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

ALL 50 STATES
Full report

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

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

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

There is a potential software error during programming.

ALL 50 STATES
Full report

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

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

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

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

ALL 50 STATES
Full report

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

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

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

There is a potential software error during programming.

ALL 50 STATES
Full report

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

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

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

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

ALL 50 STATES
Full report

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

Recall #:
86939
Lot/product code:
Lot Numbers: 20NXAC033  Additional Affected lots as of 3/17/21: 20LXAC097 20NXAC033
Recalling firm:
Fresenius Medical Care Holdings, Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

THYMOSIN BETA - 4, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0140-2021
Lot/product code:
Lot #1110202005, Exp 12/10/2020; Lot #1102202015, Exp 12/08/2020; Lot #1105202009, Exp 12/20/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

FGL, 10 MG/ML, 3 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0129-2021
Lot/product code:
Lot #1112202006, Exp 12/12/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

Pentosan Polysulfate, 300 MG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0144-2021
Lot/product code:
Lot #1110202006, exp 12/10/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

CEREBROLYSIN, 107.5 MG/ML, 10 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0139-2021
Lot/product code:
Lot #1110202004 Exp 12/10/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

THYMOSIN ALPHA, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0133-2021
Lot/product code:
Lot #110220200, 1102202009, Exp 12/09/2020; Lot #1105202009, Exp 12/20/2020; Lot #1110202008, Exp 12/10/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

GHK-CU, 10 MG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0141-2021
Lot/product code:
Lot #1030202010, Exp 11/30/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

GHRP, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0135-2021
Lot/product code:
Lot #1112202008, Exp 12/11/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

IPAMORELIN, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0134-2021
Lot/product code:
Lot # 1029202005,Exp 11/29/2020; Lot #1102202014, Exp 12/08/2020; Lot #1112202002, Exp 12/12/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

CJC-1295, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0128-2021
Lot/product code:
Lot #1029202004, Exp 11/29/2020; Lot #1102202001, 102202009, Exp 12/08/2020; Lot #1105202009, Exp 12/20/2020; Lot #1110202003, Exp 12/10/2020; Lot #1112202004, Exp 12/12/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled November 30, 2020

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

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

ALL 50 STATES
Full report

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

Recall #:
87026
Lot/product code:
Model number: Artis zee floor- 10094135 Artis zee ceiling- 10094137 Artis zee multi-purpose- 10094139 Artis zee biplane- 10094141 Artis zeego- 10280959 Artis Pheno- 10849000 Artis Q floor- 10848280 Artis Q ceiling- 10848281 Artis Q biplane- 10848282 Artis Q zeego- 10848283 Artis Q.zen floor- 10848353 Artis Q.zen ceiling- 10848354 Artis Q.zen biplane- 10848355
Recalling firm:
Siemens Medical Solutions USA, Inc
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

HIGH DOSE B12, 10 MG/ML, 10 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0142-2021
Lot/product code:
Lot #1029202007, Exp 12/29/20
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

LL-37, 2000 MCG/ML, 2 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0143-2021
Lot/product code:
Lot #1105202006, Exp 12/18/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

BPC-157, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0132-2021
Lot/product code:
Lot #1102202009, Exp 12/08/2020; Lot #1105202009, Exp 12/20/2020; Lot #1110202001, Exp 12/15/2020; Lot #1112202004, Exp 12/12/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

NANDROLONE, 200 MCG/ML, 2 ML, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0136-2021
Lot/product code:
Lot #1113202002, Exp 01/13/2021; Lot #1102202005, Exp 12/08/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

PT-141, 10 MG/ML, 2 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0130-2021
Lot/product code:
Lot #1112202006, Exp 12/12/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

DSIP, 1000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0138-2021
Lot/product code:
Lot #1111202002, Exp 12/11/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

B12 for Injection, 2 MG/ML, 10 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0137-2021
Lot/product code:
Lot #1111202001, Exp 01/11/2021
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled November 30, 2020

AOD-9604, 1200 MCG/ML, 5 ML vial The Guyer Institute of Molecular Medicine, Indianapolis, IN

Not guaranteed to be germ-free: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Full report

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

Recall #:
D-0131-2021
Lot/product code:
Lot #1029202003, Exp 11/29/2020; Lot #1110202002, Exp 12/10/2020; Lot #1112202001, Exp 12/12/2020
Recalling firm:
Advanced Nutriceuticals, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled December 2, 2020

EMBLEM MRI S-ICD pulse generators, as part of Boston Scientific S-ICD System; Model A219

Accelerated battery depletion may result in a need for device replacement earlier than expected.

ALL 50 STATES
Full report

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

Recall #:
86866
Lot/product code:
Serial numbers distributed in the United States:  100371 100467 100485 100548 100591 100641 100705 100710 100717 100742 100745 100791 100866 100868 200019 200023 200031 200043 200049 200067 200125 200126 200127 200128 200129 200152 200157 200161 200163 200167 200170 200171 200176 200181 200182 200185 200186 200187 200190 200191 200192 200195 200198 200214 200217 200224 200228 200232 200236 200239 200241 200244 200247 200251 200256 200258 200261 200262 200264 200266 200269 200276 200283 200287 200290 200291 200293 200297 200300 200301 200313 200317 200330 200331 200333 200335 200341 200347 200348 200351 200358 200359 200360 200366 200367 200368 200369 200370 200372 200373 200374 200375 200378 200381 200382 200384 200386 200388 200389 200390 200391 200394 200398 200402 200403 200406 200410 200422 200423 200425 200426 200428 200431 200435 200436 200437 200441 200442 200444 200445 200448 200449 200452 200453 200461 200465 200468 200469 200470 200471 200473 200479 200481 200482 200488 200491 200493 200497 200503 200506 200510 200511 200515 200517 200518 200519 200524 200527 200533 200535 200536 200543 200545 200546 200553 200554 200555 200556 200557 200563 200564 200567 200574 200575 200577 200579 200580 200584 200585 200587 200588 200589 200590 200591 200592 200593 200595 200598 200599 200600 200604 200605 200606 200607 200620 200624 200625 200628 200629 200631 200634 200636 200637 200641 200642 200645 200648 200651 200654 200656 200657 200658 200659 200663 200665 200667 200669 200671 200677 200679 200680 200683 200684 200685 200688 200689 200691 200692 200693 200696 200698 200702 200703 200704 200705 200707 200712 200713 200716 200717 200718 200719 200721 200723 200726 200727 200729 200730 200738 200739 200740 200741 200742 200743 200745 200746 200747 200748 200749 200750 200752 200753 200754 200755 200760 200761 200762 200763 200770 200775 200777 200778 200779 200782 200783 200786 200787 200794 200800 200801 200802 200803 200805 200806 200810 200811 200812 200814 200815 200818 200821 200822 200824 200825 200831 200832 200833 200836 200838 200839 200841 200842 200843 200844 200848 200854 200856 200865 200867 200869 200871 200874 200882 200887 200888 200889 200891 200892 200893 200896 200899 200903 200905 200906 200909 200910 200911 200913 200914 200917 200919 200923 200925 200927 200928 200930 200933 200934 200939 200945 200946 200950 200953 200954 200957 200961 200965 200966 200968 200970 200971 200972 200973 200979 200983 200986 200988 200990 200991 200992 200995 200996 200997 200998 201001 201002 201006 201009 201010 201011 201012 201013 201016 201017 201021 201024 201027 201028 201031 201032 201033 201034 201036 201041 201044 201045 201047 201048 201049 201050 201054 201055 201061 201062 201063 201064 201067 201069 201070 201071 201074 201075 201076 201077 201078 201079 201080 201084 201085 201086 201089 201090 201092 201095 201096 201098 201099 201100 201103 201104 201107 201108 201110 201112 201114 201116 201118 201119 201123 201124 201125 201126 201127 201131 201133 201134 201135 201137 201139 201143 201144 201146 201147 201148 201149 201150 201151 201152 201153 201156 201157 201160 201161 201165 201166 201167 201168 201169 201170 201171 201172 201173 201174 201176 201177 201178 201179 201180 201182 201187 201188 201189 201191 201192 201193 201194 201195 201196 201197 201198 201200 201203 201205 201206 201207 201208 201209 201210 201211 201212 201213 201214 201215 201216 201218 201219 201220 201221 201222 201223 201225 201226 201231 201232 201233 201234 201237 201238 201239 201240 201242 201243 201245 201246 201247 201248 201251 201252 201253 201254 201255 201256 201258 201259 201264 201265 201266 201267 201268 201269 201270 201272 201273 201274 201276 201277 201278 201279 201280 201281 201282 201283 201284 201286 201287 201288 201290 201291 201292 201293 201294 201295 201296 201297 201298 201299 201300 201301 201303 201306 201307 201308 201309 201312 201314 201315 201316 201318 201319 201320 201322 201323 201324 201325 201326 201328 201329 201331 201332 201333 201335 201337 201338 201339 201340 201341 201342 201343 201345 201346 201348 201349 201353 201396 201400 201402 201404 201405 201406 201408 201409 201410 201413 201416 201419 201420 201421 201422 201423 201424 201428 201431 201434 201435 201436 201438 201439 201440 201441 201444 201451 201452 201454 201456 201459 201460 201462 201463 201464 201466 201467 201468 201471 201476 201477 201479 201480 201481 201486 201487 201488 201491 201498 201501 201510 201512 201513 201514 201515 201516 201517 201521 201525 201533 201534 201537 201539 201544 201545 201548 201551 201554 201555 201556 201557 201558 201562 201563 201564 201565 201567 201568 201570 201571 201572 201579 201580 201581 201585 201587 201589 201592 201598 201599 201600 201602 201606 201612 201619 201622 201623 201626 201631 201634 201637 201640 201641 201642 201643 201645 201646 201648 201651 201655 201658 201661 201662 201664 201667 201677 201678 201679 201684 201685 201686 201687 201688 2… (truncated, 151353 characters total — see the official FDA record for the full value)
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)