State

Utah product recalls

20,371 recalls have nationwide distribution and so reach Utah. 0 additional recalls listed Utah specifically in their distribution scope.

About recalls in Utah

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Utah consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

15951–15975 of 20371

ModerateFDA (Drugs)·D-1392-2022·2022-08-31
Pain Reliever Caplets Recalled for Improper Storage Temperature
Over-the-counter pain reliever caplet products from Family Dollar stores are being recalled because they were stored outside proper temperature conditions.
Product
READY IN CASE PAIN RELIEVER PM CAPLET 100 CT SKU 902381 GOOD SENSE PAIN RELIEVER APAP 500MG CAPLET 250CT SKU 902332 READY IN CASE PM PAIN RELIEVER CAPLET 50 CT SKU 913982 GOOD SENSE PAIN RELIEVER APAP ES 500 CT SKU 999029 GOOD SENSE PAIN RELIEVER CAPLET 100 CT SKU 913890
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1439-2022·2022-08-31
MIDOL and Related OTC Menstrual Relief Products Recalled for Temperature Storage Deviation
Family Dollar Stores recalled MIDOL COMPLETE, QP MENSTRUAL RELIEF, and QP PMS FORMULA caplets distributed April–June 2022 due to CGMP deviations from improper storage temperature.
Product
MIDOL COMPLETE CAPLET 16 CT SKU 913028 QP MENSTRUAL RELIEF COMPLETE CAPLET 16CT SKU 999982 QP PMS FORMULA CAPLET 32 CT SKU 913232 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1567-2022·2022-08-31
Stryker SWANSON Finger Joint Implant Incorrect Sizing Label on Carton
Wright Medical Technology is recalling 17 Stryker SWANSON Finger Joint Implants (size 00) due to incorrect sizing labels applied to carton packaging. Devices with lot numbers 1728375 and 1728376 were distributed across multiple US states and internationally.
Product
Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1377-2022·2022-08-31
Dial Men's Eucalyptus Body Wash Recalled Due to Storage Temperature Deviation
Family Dollar Stores is recalling Dial Men's Eucalyptus Body Wash 20 fl oz due to improper storage temperature conditions during distribution.
Product
DIAL MENS EUCALYPTUS AB BODY WASH 20 FLOZ SKU 2096030 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1609-2022·2022-08-31
Medline Catheter Insertion Tray Recalled for Temperature Exposure During Manufacturing
Mckesson Medical-Surgical is recalling Medline catheter insertion trays (Model DYND10160) due to temperature excursions at the manufacturing facility that may have affected product effectiveness. Affected units were distributed nationwide between June and September 2021.
Product
MEDLINE INDUSTRIES Medline Catheter Insertion Tray Medline Foley Without Catheter Without Balloon Model Number: DYND10160
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1389-2022·2022-08-31
Lidocaine arthritis topical product recalled due to improper storage
Family Dollar Stores is recalling Lidocaine Arthritis and Sport wintergreen liniment (16 fl oz, SKU 902929) distributed nationwide April 30–June 10, 2022, due to improper storage temperature conditions.
Product
LIDOCAINE ARTHRITIS AND SPORT WNTGRN 16 FLOZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1396-2022·2022-08-31
Preferred Urinary Pain Relief Product Recalled for Improper Storage Conditions
Family Dollar Stores is recalling Preferred Urinary Pain Relief Max Strength due to CGMP violations involving improper storage temperature. Product was distributed nationwide April 30 through June 10, 2022.
Product
PREFERRED URINRY PN RLF MAX STRNGTH 12 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1573-2022·2022-08-31
Mizuho OSI Femoral Hooks Recalled for Incorrect Model Etching
Mizuho OSI is recalling one batch of regular femoral hooks that were etched with an incorrect model designation. The recalled batch contains 13 devices distributed in the United States and Canada.
Product
HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1631-2022·2022-08-31
Cooper Surgical Milex Pessary Recalled for Temperature Exposure During Storage
Mckesson Medical-Surgical is recalling Cooper Surgical Milex Pessary Ring products stored at elevated temperatures from June through August 2021, which may have degraded product effectiveness.
Product
COOPER SURGICAL Milex PESSARY, RING MILEX INCONT FLEXIBLE SZ6 1 3/4" Catalog # MXPCON06
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1441-2022·2022-08-31
Family Dollar Stye Eye Ointment Recalled Due to Improper Storage
Family Dollar is recalling Stye Eye Ointment 0.125 oz due to manufacturing deviations. The product was held outside appropriate storage temperature conditions.
Product
STYE EYE OINTMENT 0.125 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1416-2022·2022-08-31
Mylanta Max Strength Classic flavor antacid recalled for improper storage conditions
Mylanta Max Strength Classic flavor antacid (12 fl oz, SKU 999844) has been recalled due to improper storage temperature conditions. The product was distributed nationwide to Family Dollar Stores from April 30 to June 10, 2022.
Product
MYLANTA MAX STRENGTH CLASSIC FLVR 12 FLOZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1409-2022·2022-08-31
Doctor Teal's Epsom Salt Recalled for Improper Storage Conditions
Family Dollar Stores is recalling Doctor Teal's Pure Epsom Salt packages distributed April 30–June 10, 2022 due to improper storage temperature conditions.
Product
DOCTOR TEALS PURE EPSOM SALT UNSCENTED 6 LBS SKU 999355 Ready in case EPSOM SALTS 2 LB SKU 909223 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1436-2022·2022-08-31
Lidocaine Cream Products Recalled for Improper Storage Conditions at Family Dollar
Family Dollar is recalling Aspercreme with Lidocaine Creme (SKU 999852) and Icy Hot Lidocaine Cream (SKU 999853) distributed April 30 through June 10, 2022 nationwide due to improper storage temperature conditions.
Product
ASPERCREME WITH LIDOCAINE CREME 1.75 OZ SKU 999852 ICY HOT LIDOCAINE CREAM 1.75 OZ SKU 999853 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1366-2022·2022-08-31
Personal Care Lotions Recalled Due to Improper Storage Temperature
Family Dollar Stores is recalling multiple lotion products that were held outside appropriate storage temperatures. The affected brands include Dermasil, Aveeno, and Vaseline products distributed from April 30 through June 10, 2022.
Product
Dermasil Dry Skin Treatment 10 OZ SKU 2098068 Aveeno Daily Moisturizing Lotion 5 OZ SKU 2005444 Aveeno Baby Daily Moistue Lotion 8 OZ SKU 900016 Vaseline Mens Extra Strength Body and Face Lotion 10 OZ SKU 2003674 distributed to specific Family Dollar Stores 04/30/2022 thro
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1380-2022·2022-08-31
Orajel Cold Sore Pain Cream Recalled for Improper Storage Conditions
Orajel Cold Sore Pain Cream 1.25 fl. oz. was recalled because it was stored outside appropriate temperature conditions. The product was distributed to Family Dollar Stores from April 30 through June 10, 2022.
Product
Orajel Cold Sore Pain Cream 1.25 fl. oz. distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1419-2022·2022-08-31
PEPCID antacid tablets recalled for improper storage temperature handling
Family Dollar Stores is recalling three PEPCID antacid products due to improper storage temperature conditions at specific Family Dollar locations from April through June 2022.
Product
PEPCID COMPLETE CHEWABLE TAB BERRY 8CT SKU 903365 PEPCID AC MAXIMUM STRENGTH TABLET 25 CT SKU 902063 PEPCID AC MAXIMUM STRENGTH TABLET 8 CT SKU 914773 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1425-2022·2022-08-31
Family Dollar Laxative Products Recalled for Improper Storage Conditions
Family Dollar recalls two bisacodyl laxative products (SKUs 902449 and 915221) distributed to specific stores from April to June 2022 due to storage temperature deviations affecting product quality.
Product
QP LAXATIVE BISACODYL 5 MG TABLET 50 CT SKU 902449 QP WOMEN LAXATIVE BISCODYL TABLET 25 CT SKU 915221 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1379-2022·2022-08-31
Dandruff Shampoo Products Recalled for Improper Storage Temperature Conditions
Family Dollar Stores is recalling multiple dandruff shampoo brands sold between April and June 2022 because they were stored at improper temperatures. No illnesses have been reported.
Product
DOCTOR DANDRUF 2N1 SHAMP CLN APL 13.5FLOZ SKU 2005726 SUAVE 2N1 MENS CC ANTI DNDRF SHMP 28 FLOZSKU 2006512 MANE N TAIL 2 IN 1 ANTI DANDRUFF 12 FL OZ SKU 2024652 HEAD AND SOULDERS 2N1 SMOOTH SILKY 12.8 FL OZ SKU 2097272 DOCTOR MED DANDRUFF TREAT 11 FL OZ SKU 2005531 HEAD
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1445-2022·2022-08-31
Nicorette Gum Recalled Due to Improper Storage Temperature Conditions
Family Dollar Stores is recalling NICORETTE GUM WHITE ICE MINT 4 MG distributed from April 30 through June 10, 2022. The product was held outside appropriate storage temperature conditions.
Product
NICORETTE GUM WHITE ICE MINT 4 MG 20 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1596-2022·2022-08-31
FDA Recalls Heparin Sodium Prefilled Syringes Due to Heat Damage
Mckesson Medical-Surgical Inc. is recalling Excelsior Heparin Sodium prefilled syringes that may have been damaged by temperature excursions during manufacturing, potentially affecting their effectiveness. The recall covers lots received between June and September 2021.
Product
Excelsior Heparin Sodium, Porcine, Preservative Free 100 U / mL Solution Prefilled Syringe, Partial Fill 5 mL Fill in 10 mL Syringe Model Number: 513604
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1619-2022·2022-08-31
McKesson Medefil Normal Saline IV Flush Syringes Recalled for Temperature Exposure
McKesson is recalling Medefil Normal Saline IV Flush Syringes (Models MIS-1130 and 191-MIS-1130) due to facility temperature excursions between June and August 2021. Products received through September 30, 2021 may have impaired effectiveness from temperature exposure prior to delivery.
Product
a. Medefil Normal Saline IV Flush Syringe NORMAL SALINE FLUSH, SYR 10ML/12ML (60/BX 16BX/CS), Model Number: MIS-1130. b. MEDEFIL INC McKesson SALINE IV FLUSH, SYR NORMAL 10ML/12ML .9% (60/BX 16BX/CS) Model Number: 191-MIS-1130.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1407-2022·2022-08-31
Good Sense Hemorrhoid Products Recalled for Improper Storage Conditions
Good Sense Hemorrhoid Ointment and Wipes sold at Family Dollar stores from April through June 2022 are being recalled due to storage outside appropriate temperature conditions. No illnesses have been reported.
Product
GOOD SENSE HEMORRHOID OINTMENT 2 OZ SKU 910325 GOOD SENSE HEMORRHOIDAL WIPES 48 CT SKU 902260 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1385-2022·2022-08-31
Benadryl Extra Strength Cream Recalled for Improper Storage Conditions
Family Dollar Stores is recalling Benadryl Extra Strength Cream 1 oz distributed from April 30 through June 10, 2022, because the product was held outside appropriate storage temperature conditions. No illnesses have been reported.
Product
BENADRYL EXTRA STRENGTH CREAM 1 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1589-2022·2022-08-31
Drugs of Abuse Test Kits Recalled Due to Temperature Exposure
McKesson Medical-Surgical is recalling multiple brands of drugs of abuse test kits because temperature excursions prior to delivery may have reduced product effectiveness.
Product
Drugs of Abuse Tests: a. Wondfo Tdip Drugs of Abuse Test Tdip Single Drug Fentanyl (FEN) Urine Sample 25 Tests. Model Number: AWFTY-114. b. Alere Drugs of Abuse Test E-Z Split Key Cup 12-Drug Panel AMP, BAR, BUP, BZO, COC, mAMP/MET, MDMA, MOP, MTD, OXY, PPX, THC Urine S
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·22210·2022-08-25
Stand-up Paddleboard Paddles Recalled for Puncture and Laceration Risk
Agit Global stand-up paddleboard paddles can suddenly break mid-shaft during use, exposing sharp edges. About 124,000 units sold nationwide from 2015–2020 pose a risk of serious puncture or laceration injuries.
Product
Paddles sold with stand-up paddleboards
Category
Consumer Product
Distribution
Distributed nationwide