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Recalls affecting Rhode Island

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

16,286 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 March 25, 2021

Intellis Model 97755 Recharger - Product Usage: designed to charge the following Medtronic rechargeable neurostimulators: Intellis with AdaptiveStim Technology Model 97715 Implanted Neurostimulator Intellis Model 97716 Implanted Neurostimulator.

There is a potential for unintended heating that can occur with the Intellis Model 97755 Recharger.

ALL 50 STATES
Full report

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

Recall #:
87674
Lot/product code:
All serial numbers
Recalling firm:
Medtronic Neuromodulation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled March 26, 2021

Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number: 10094137

Some Artis zee ceiling systems show an increased abrasion of the cabling at the cable outlet of the inner C-arm, the limited functionality may not be sufficient to continue with treatment as planned. This may result in a situation where it is necessary to cancel clinical treatment or to continue treatment on an alternative system.

ALL 50 STATES
Full report

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

Recall #:
87672
Lot/product code:
Serial Numbers: 125000 125001 125002 125003 125004 125005 125006 125008 125009 125010 125011 125013 125015 125016 125017 125019 125021 125022 125023 125024 125100 125105 125106 125108 125109 125112 125113 125115 125116 125117 125118 125119 125201 125202 125204 125205 125208 125209 125210 125211 125212 125213 125214 125216 125219 125222 125223 125226 125227 125228 125229 125230 125231 125232 125233 125235 125238 125239 125240 125241 125243 125244 125245 125249 125250 125251 125253 125254 125255 125256 125257 125260 125262 125263 125265 125267 125268 125269 125270 125273 125274 125275 125276 125278 146104 146107 146111 146116 146118 146119 146121 146123 146130 146136 146137 146138 146139 146140 146144 146147 146149 146150 146152 146156 146158 146161 146164 146166 146168 146169 146170 146173 146174 146175 146176 146178 146179 146181 146183 146184 146186 146187 146188 146189 146193 146197 146205 146206 146212 146217 146218 146219 146220 146232 146233 146235 146238 146239 146241 146242 146245 146251 146257 146260 146263 146264 146266 146267 146272 146274 146277 146279 146286 146287 146289 146290 146292 146293 146297 146298 146299 146305 146308 146313 146320 146322 146323 146324 146326 146327 146333 146334 146335 146338 146340 146341 146342 146343 146348 146352 146354 146357 146361 146365 146366 146368 146369 146370 146372 146373 146382 146386 146388 146391 146393 146394 146395 146397 146398 146406 146407 146410 146411 146424 146427 146612 146618 146619 146623 146627 146630 146631 146632 146634 146635 146637 146643 146644 146650 146652 146656 146658 146659 146663 146667 146669 146676 146677 146679 146688 146690 146691 146692 146694 146696 146697 146698 146700 146701 146703 146705 146709 146710 146711 146712 146713 146714 146715 146717 146719 146720 146721 146724 146727 146729 146731 146732 146733 146735 146738 146740 146741 146742 146747 146748 146750 146753 146755 146756 146758 146759 146761 146766 146774 146775 146776 146779 146780 146781 146782 146784 146786 146793 146795 146797 146798 146801 146803 146806 146809 146811 146812 146814 146817 146818 146821 146825 146827 146828 146829 146830 146833 146839 146846 146851 146855 146857 146860 146861 146863 146866 146867 146868 146869 146871 146877 146881 146883 146886 146887 146888 146895 146896 146898 146899 146905 146908 146909 146912 146915 146918 146919 146925 146927 146928 146929 146932 146933 146934 146935 146937 146939 146940 146942 146945 146946 146948 146952 146955 146957 146959 146960 146963 146964 146965 146969 146971 146972 146973 146975 146976 146977 146980 146983 146986 146987 146988 146991 146993 146994 146996 147009 147023 147024 147025 147027 147029 147030 147031 147035 147036 147042 147043 147044 147046 147047 147049 147059 147075 147078 147079 147081 147083 147084 147087 147088 147089 147093 147094 147096 147098 147100 147103 147105 147106 147107 147109 147113 147114 147119 147120 147121 147123 147124 147155 147157 147164 147165 147167 147168 147171 147172 147174 147175 147177 147186 147188 147189 147190 147193 147196 147200 147203 147205 147207 147210 147214 147216 147233 147234 147235 147236 147238 147239 147241 147243 147249 147250 147251 147252 147253 147254 147255 147264 147265 147268 147285 147287 147295 147296 147301 147303 147304 147307 147357 147363 147364 147365 147371 147372 147373 147500 147507 147514 147515 147516 147526 147528 147541 147552 147553 147557 147558 147559 147561 147562 147573 147577 147581 147583 147585 147587 147601 147604 147608 147612 147620 147621 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(truncated, 5419 characters total — see the official FDA record for the full value)
Recalling firm:
Siemens Medical Solutions USA, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 29, 2021

69MODE Blue 69 capsule, packaged in 10-count box, Nuri Trading LLC

Marketed Without An Approved NDA/ANDA: Product found to be tainted with not listed on the label tadalafil and sildenafil, two FDA approved drugs making it an unapproved drug for which the safety and efficacy have not been established and therefore subject to recall.

ALL 50 STATES
Full report

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

Recall #:
D-0688-2021
Lot/product code:
all lots within expiry
Recalling firm:
Nuri Trading LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled March 29, 2021

Philips Xper Flex Cardio (FC2010, Procedure Room and FC2020, Bedside Monitor) devices - intended for use by professional healthcare providers for complete physiologic/hemodynamic monitoring Service numbers associated with FC2010: Xper Flex Cardio 2010 Rev A 453564241901 Xper Flex Cardio 2010 Rev B 453564483321 Flex Cardio FC2010 Rev C 453564621791 Xper Flex Cardio 2010 REV C RUEXCHANGE 453564675021 Xper Flex Cardio 2010 Rev D 453564669081 Xper Flex Cardio 2010 Rev D Russia 453564674581 Xper Flex Cardio FC2010 Rev E 453564845841 Xper Flex Cardio 2010 Rev E Russia 453564845881 Service numbers associated with FC2020: Xper Flex Cardio 2020 Rev A 453564241911 Xper Flex Cardio 2020 Rev B 453564483331 Flex Cardio FC2020 Rev C 453564621801 Xper Flex Cardio 2020 Rev D 453564675001 Xper Flex Cardio FC2020 Rev E 453564845861 Software version number: 1.5.19 and 1.6.8

Performance issues with the Xper Flex Cardio Physio Monitoring System include: potential delay of up to 10 seconds in displaying ECG, invasive blood pressure and other parameters; patient weight is rounded to the nearest whole kilogram;Xper IM software used with the Xper Flex Cardio Physio Monitoring System may periodically crash; No SpO2 numeric or plethysmography is displayed when SpO2 is connected o the Flex Cardio device; display of certain data from the FC2010 becomes frozen, i.e., waveforms cease sweeping and updating and the ECG, IBP, and respiration numeric values cease to update;e ECG, IBP, and respiration waveforms become flat lines and no audible alarms are produced for HR and IBP, upon start up, an unexpected non physiological ECG waveform, erratic heart rate numeric value, and non-physiological display of any other active waveforms may appear on the Boom Monitor

ALL 50 STATES
Full report

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

Recall #:
87732
Lot/product code:
Service Number/ UDI # 453564241901 (01)00884838082113; 453564241911 (01)00884838082113; 453564483321 (01)00884838082113; 453564483331 (01)00884838083516; 453564621791 (01)00884838084902; 453564621801 (01)00884838084919; 453564845881 (01)00884838095052; 453564675021 (01)00884838103245; 453564669081 (01)00884838083820; 453564675001 (01)00884838086005; 453564674581 (01)00884838083820; 453564845841 (01)00884838093645; 453564845861 (01)00884838093652
Recalling firm:
Philips North America Llc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 29, 2021

Thumbs Up 7 Black 25K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

Marketed Without An Approved NDA/ANDA: Product found to be tainted with not listed on the label tadalafil, an FDA approved drug making this an unapproved drug for which the safety and efficacy has not been established and therefore subject to recall.

ALL 50 STATES
Full report

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

Recall #:
D-0686-2021
Lot/product code:
all lots within expiry
Recalling firm:
Nuri Trading LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 29, 2021

Thumbs Up 7 White 11K capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

Marketed Without An Approved NDA/ANDA: Product found to be tainted with not listed on the label tadalafil sildenafil, and vardenafil, FDA approved drugs making them an unapproved drug for which the safety and efficacy have not been established and therefore subject to recall.

ALL 50 STATES
Full report

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

Recall #:
D-0687-2021
Lot/product code:
all lots within expiry
Recalling firm:
Nuri Trading LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 29, 2021

Shogun-X 7000 capsule, packaged in a) 1-count blister card and b) 10-count box, Nuri Trading LLC

Marketed Without An Approved NDA/ANDA: Product found to be tainted with not listed on the label tadalafil and sildenafil, two FDA approved drugs making them unapproved drugs for which the safety and efficacy have not been established and therefore subject to recall.

ALL 50 STATES
Full report

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

Recall #:
D-0685-2021
Lot/product code:
all lots within expiry
Recalling firm:
Nuri Trading LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled March 30, 2021

PremierZen Platinum 5000, Packaged in paper packaging with a pill blister, 1 capsule per box, Distributed by New Premier Group Los Angeles CA 90006

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

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-0353-2021
Lot/product code:
Lot #: GATCO 01671, Exp Date 12/30/2024 Serial # 728175421856
Recalling firm:
Na Na Collection
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled March 30, 2021

Triple SupremeZen Gold 3500, Packaged in paper packaging with a pill blister,1 capsule per box, Distributed by VIEW LIFE Distributors Los Angeles CA 90005 UPC 7 15122 05089 4

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

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-0354-2021
Lot/product code:
Lot #: GATCO 1805, Exp. Date 12/30/2024 Serial # 715122050894
Recalling firm:
Na Na Collection
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled March 31, 2021

Imperial Platinum 2000, 1 capsule, UPC 718122040702

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

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-0371-2021
Lot/product code:
All
Recalling firm:
QMart
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled March 31, 2021

Guanfacine Extended-Release Tablets 2 mg,100-count bottles, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326, NDC 60505-3928-1, UPC 3 60505 39281 0

Cross Contamination with Other Product: Product is being recalled due to Trace Amounts of Quetiapine Fumarate

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-0324-2021
Lot/product code:
Lot #: RX1662, RX1663, RX1664 Exp. 11/2022
Recalling firm:
Apotex Corp.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled March 31, 2021

IMPERIAL GOLD 2000, Male Sexual Performance Enhancement, 1 Capsule, UPC 718122040702

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

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-0368-2021
Lot/product code:
All
Recalling firm:
QMart
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled March 31, 2021

PremierZen Extreme 3000, Male Sexual Performance Enhancement, 1 Capsule, UPC 728175421887

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

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-0369-2021
Lot/product code:
All
Recalling firm:
QMart
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled March 31, 2021

Burro en Primavera, 2 capsules, UPC 638632431055

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

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-0370-2021
Lot/product code:
All
Recalling firm:
QMart
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 1, 2021

Power Wheelchair

Seat baseplate pin has broken in the field.

ALL 50 STATES
Full report

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

Recall #:
87673
Lot/product code:
Gemini PWC- Model Number: P301; Part No: P30111ARMU; Serial Numbers: MU200900398, MU200401050, MU200900415, MU200401058, MU200401064, MU200401069, MU200401067, MU200401060, MU200900417, MU200900410, MU200401059, MU200401063, MU200401068, MU200401062, MU200401056, MU200401065, MU200401055, MU200401051, MU200900404, MU200900409, MU200900399, MU200900416, MU200900405, MU200900407, MU200401061, MU200401066, MU200401054, MU200401052 Gemini PWC - Model Number: P301; Part No: P3017-ARMU; Serial Numbers: MU200700022, MU200800669, MU200700024, MU200800660, MU200800665, MU200800661, MU200800664, MU200800668, MU200800663, MU200700028, MU200700021, MU200800659, MU200800667, MU200800662, MU200700026, MU200700025, MU200700023, MU200700027 Gemini PWC - Model Number: P301; Part No: P3017-SBMU; Serial Numbers: MU200700036, MU200800671, MU200800672, MU200800675, MU200800678, MU200800674, MU200700033, MU200800676 Regal PWC Model Number: P310; Part No: P310A-ARMUB; Serial Numbers: MU200900199, MU200900881, MU200900890, MU200900204, MU200900246, MU200900247, MU200900208 Vision CF PWC Model Number: P322; Part No: P322A3ARMUB; Serial Numbers: MU200600861, MU200600524, MU200600850, MU200600529, MU200600555, MU200600871, MU200600840, MU200600863, MU200600547, MU200600014, MU200600018, MU200600022, MU200600020, MU200600267, MU200600275, MU200600256, MU200600258, MU200600272, MU200600278, MU200600264, MU200600285, MU200600281, MU200600289, MU200900844, MU200600049, MU200600007, MU200600017, MU200600001, MU200600047, MU200600036, MU200600034, MU200600844, MU200600825, MU200600826, MU200600827, MU200600050, MU200600544, MU200600545, MU200600549, MU200600527, MU200600560, MU200600531, MU200600530, MU200600537, MU200600536, MU200600546, MU200600550, MU200600554, MU200900842, MU200900849, MU200900850, MU200900845, MU200600495, MU200600501, MU200600496, MU200600494, MU200600502, MU200600513, MU200600539, MU200600503, MU200600514, MU200600504, MU200600500, MU200600538, MU200600535, MU200600026, MU200600011, MU200600042, MU200600870, MU200600862, MU200600257, MU200600265, MU200600835, MU200600851, MU200600852, MU200600866, MU200600284, MU200600004, MU200600263, MU200600269, MU200600277, MU200600286, MU200600002, MU200600003, MU200600039, MU200600035, MU200600043, MU200600019, MU200600869, MU200600864, MU200600857, MU200600860, MU200600048, MU200600045, MU200900846, MU200900843, MU200900848, MU200600838, MU200600841, MU200600831, MU200600858, MU200600259, MU200600262, MU200600509, MU200600023, MU200600290, MU200600270, MU200600859, MU200600021, MU200600512, MU200600532, MU200600009, MU200600846, MU200600839, MU200600848, MU200600830, MU200600013, MU200600542, MU200600842, MU200600518, MU200600492, MU200600024, MU200600027, MU200600040, MU200600280, MU200600853, MU200600855, MU200600854, MU200600012, MU200600038, MU200600015, MU200600558, MU200600553, MU200600559, MU200600540, MU200600548, MU200600525, MU200600497, MU200600498, MU200600528, MU200600491, MU200600493, MU200600030, MU200600543, MU200600541, MU200600505, MU200600872, MU200900847, MU200600834, MU200600833, MU200600276, MU200600028, MU200600025, MU200600873, MU200600867, MU200600868, MU200600031, MU200600865, MU200600032, MU200600033, MU200600029, MU200600287 Vision CF PWC Model Number: P322; Part No: P322A4ARMUB; Serial Numbers: MU200600082, MU200600076, MU200600089, MU200600078, MU200600087, MU200600065, MU200600067, MU200600063, MU200600093, MU200600401, MU200600305, MU200600091, MU200600075, MU200900859, MU200600097, MU200600070, MU200600315, MU200900851, MU200900860, MU200900853, MU200900861, MU200600410, MU200600389, MU200600592, MU200600590, MU200600317, MU200600293, MU200600320, MU200600295, MU200600292, MU200600064, MU200600098, MU200600068, MU200600061, MU200600085, MU200600062, MU200600096, MU200600072, MU200900855, MU200900852, MU200600321, MU200600308, MU200600298, MU200600304, MU200600069, MU200600084, MU200600299, MU200600081, MU200600066, MU200600411, MU200600071, MU200600400, MU200600090, MU200600296, MU200600312, MU200600311, MU200600301, MU200600088, MU200600316, MU200600323, MU200600306, MU200600324, MU200600325, MU200600297, MU200600303, MU200600310, MU200600094, MU200900857, MU200900856, MU200900854, MU200900858, MU200600079, MU200600099, MU200600080, MU200600092, MU200600318, MU200600313, MU200600077, MU200600095 Vision Sport PWC Model Number: P326; Part No: P326AIARMUB; Serial Numbers: TMU200401384, TMU200401397, TMU200401407, TMU200401379, TMU200401380, TMU200401298, TMU200401299, TMU200401300, TMU200401302, TMU200401305, TMU200401306, TMU200401307, TMU200401311, TMU200401314, TMU200401316, TMU200401318, TMU200401319, TMU200401320, TMU200401321, TMU200401322, TMU200401323, TMU200401324, TMU200401429, TMU200401402, TMU200401403, TMU200401405, TMU200401304, TMU200401439, TMU200401432, TMU200401381, TMU200401392, TMU200401441, TMU200401438, TMU200401417, TMU200401427, TMU200401416, TMU200401450, TMU200401297, TMU200401317, TMU200401310, TMU200401413, TM… (truncated, 43178 characters total — see the official FDA record for the full value)
Recalling firm:
Merits Holdings Co. dba Merits Health Products, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled April 1, 2021

Scooter

Seat baseplate pin has broken in the field.

ALL 50 STATES
Full report

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

Recall #:
87673
Lot/product code:
Pioneer 3 Scooter - Model Number: S131; Part No: S13152ARMU; Serial Numbers: MU200900928, MU200600612, MU200600610, MU200600887, MU200600621, MU200600620, MU200600619, MU200600618, MU200600608, MU200600616, MU200600609, MU200600607, MU200600615, MU200600613, MU200900930, MU200600892, MU200600874, MU200600889, MU200600877, MU200600617, MU200600888, MU200600876, MU200600883, MU200600879, MU200600885, MU200900923, MU200600886, MU200600893, MU200600890, MU200600611, MU200600875 Pioneer 3 Scooter - Model Number: S131; Part No: S13152SBMU; Serial Numbers: MU200900944, MU200900942 Pioneer 4 Scooter - Model Number: S141; Part No: S14151ARMU; Serial Numbers: MU200900956, MU200900953 Pioneer 4 Scooter - Model Number: S141; Part No: S14152ARMU; Serial Numbers: MU200800943, MU200600346, MU200600353, MU200600357, MU200800940, MU200900961, MU200801127, MU200801132, MU200800947, MU200600360, MU200800938, MU200801131, MU200600358, MU200600359, MU200600344, MU200801134, MU200600354, MU200600356, MU200600351, MU200600345, MU200600355, MU200600348, MU200801122, MU200801128, MU200900971, MU200600347, MU200600361, MU200600352, MU200600349, MU200600350, MU200800931, MU200800951, MU200800949, MU200801121, MU200800941, MU200800939, MU200800942, MU200801133, MU200801125, MU200900970, MU200801123 Pioneer 4 Scooter - Model Number: S141; Part No: S14152SBMU; Serial Numbers: MU200800952, MU200501029, MU200500382, MU200501033, MU200500381, MU200501039, MU200500363, MU200500359, MU200801161, MU200500372, MU200801157, MU200501031, MU200500364, MU200501044, MU200501042, MU200800962, MU200500378, MU200601118, MU200601123, MU200601112, MU200601110, MU200601111, MU200800957, MU200801152, MU200800976, MU200601114, MU200601121, MU200601126, MU200800975, MU200801168, MU200901022, MU200501032, MU200501046, MU200901029, MU200901020, MU200500376, MU200501028, MU200501036, MU200501041, MU200501037, MU200501040, MU200601125, MU200601120, MU200501047, MU200501038, MU200501043, MU200501034, MU200501035, MU200501030, MU200601116, MU200601117, MU200601115, MU200901004, MU200901023, MU200901007, MU200901014, MU200901008, MU200901016, MU200901000, MU200601113, MU200500365, MU200500373, MU200500371, MU200500361, MU200500374, MU200500367, MU200800973, MU200500360 Pioneer 1 Scooter - Model Number: S235; Part No: S2354-ARMUB; Serial Numbers: MU200600053, MU200600052, MU200600051, MU200600054 Pioneer 1 Scooter - Model Number: S235; Part No: S2354-SBMUB; Serial Numbers: MU200600056, MU200600058, MU200600059 Pioneer 2 Scooter - Model Number: S245; Part No: S2454-ARMUB; Serial Numbers: MU200400958, MU200400969, MU200601135, MU200400960, MU200400967, MU200400968, MU200400965, MU200400964, MU200400966, MU200400962, MU200400963 Pioneer 2 Scooter - Model Number: S245; Part No: S2454-SBMUB; Serial Numbers: MU200400975, MU200400988, MU200400979 Pioneer 9 Scooter - Model Number: S331; Part No: S331-1ARMU; Serial Numbers: MU200801178, MU200700070, MU200700075, MU200700076, MU200700069, MU200801188 Pioneer 10 Scooter - Model Number: S341; Part No: S341-1ARMU; Serial Numbers: MU200800993, MU200800992, MU200800991, MU200800994, MU200800979, MU200800977, MU200800983, MU200800989, MU200800995, MU200800990 Silverado Extreme Scooter - Model Number: S940; Part No: S940A-SDMU; Serial Numbers: MU200800528, MU200700079, MU200800531, MU200800526, MU200800535, MU200700085, MU200700081 Silverado Scooter - Model Number: S941; Part No: S941A1SVMU; Serial Numbers: MU200800538
Recalling firm:
Merits Holdings Co. dba Merits Health Products, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenMilkSoyWheatUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE COOKIES N CREAM DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89836 8 & 5lb, UPC 6 49241 87832 5 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

Full report

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

Recall #:
F-0502-2021
Lot/product code:
2lb - All EXP DATES up to and including 10/2023 5lb - All EXP DATES up to and including 09/2021
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenMilkSoyWheatUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE CHOCOLATE FUDGE POP DIETARY SUPPLEMENT NET WT. 2lb jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071 UPC 8 11836 02223 0

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

Full report

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

Recall #:
F-0499-2021
Lot/product code:
2lb - All EXP DATES up to and including 05/2023
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled April 3, 2021

HI-TECH PHARMACEUTICALS PRECISION PROTEIN COOKIES & CREAM NET WT 2lbs (907g) container UPC 8 11836 02341 1 & 5lbs. (2.2kg) UPC 8 11836 02349 7 manufactured by Hi-Tech Pharmaceuticals, 6015-B Unity Dr. Norcross, GA

During an inspection by the FDA the firm was notified by FDA that the product contains contains wheat but the label states it is "Gluten Free".

Full report

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

Recall #:
F-0511-2021
Lot/product code:
2lb - All EXP DATES up to and including 12/2022 5lb - All EXP DATES up to and including 10/2023
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenMilkSoyWheatUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE CHOCOLATE MILKSHAKE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89876 4 & 5lb, UPC 6 49241 87830 8 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

Full report

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

Recall #:
F-0500-2021
Lot/product code:
2lb - All EXP DATES up to and including 04/2023 5lb - All EXP DATES up to and including 04/2023
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenMilkSoyWheatUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE SMORES DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89002 7 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

Full report

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

Recall #:
F-0505-2021
Lot/product code:
2lb - All EXP DATES up to and including 06/2023
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenMilkEggSoyWheatUndeclaredRecalled April 3, 2021

IFN iFORCE NUTRITION MASS GAINZ PROTEIN MATRIX BROWN SUGAR MAPLE OATMEAL COOKIE NET WT 2.2 KG/4.85 LBS container UPC 8 19500 01010 1 Mfg. For Dist. By Trib?????? Enterprises, LLC Vista, CA 92081

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label egg, milk, wheat & soy.

Full report

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

Recall #:
F-0510-2021
Lot/product code:
4.85lb - All EXP DATES up to and including 01/2024 10lb - All EXP DATES up to and including 09/2021
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenMilkSoyWheatUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE CINNAMON GRAHAM CRACKER DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89001 0 & 5lb, UPC 6 49241 87831 5 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

Full report

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

Recall #:
F-0501-2021
Lot/product code:
2lb - All EXP DATES up to and including 06/2022 5lb - All EXP DATES up to and including 09/2021
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenMilkSoyWheatUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE ORANGE CREAMSICLE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89856 6 & 5lb, UPC 6 49241 87833 9 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

Full report

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

Recall #:
F-0504-2021
Lot/product code:
2lb - All EXP DATES up to and including 12/2022 5lb - All EXP DATES up to and including 12/2022
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenMilkSoyWheatUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE VANILLA MILKSHAKE DIETARY SUPPLEMENT NET WT. 2LB, UPC 6 49241 89886 5 & 5lb, UPC 6 49241 87836 0 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

Full report

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

Recall #:
F-0508-2021
Lot/product code:
2lb - All EXP DATES up to and including 09/2023 5lb - All EXP DATES up to and including 12/2021
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)