State
20,364 recalls have nationwide distribution and so reach Idaho. 0 additional recalls listed Idaho specifically in their distribution scope.
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 Idaho 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.
Family Dollar Stores is recalling Dial Men's Eucalyptus Body Wash 20 fl oz due to improper storage temperature conditions during distribution.
Family Dollar Stores is recalling QP Cold Multi-Symptom Day/Night medication distributed April 30–June 10, 2022, to select stores because the product was held at incorrect temperatures. Consumers should return the product to the store for a refund.
Family Dollar Stores recalled two antifungal products due to storage temperature deviations. The products may have been compromised in effectiveness due to failure to maintain proper 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.
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.
Family Dollar Stores is recalling Vaseline Eczema Calming Therapy Cream (6.8 oz) distributed nationwide from April 30 to June 10, 2022, because the product was held outside appropriate storage temperature conditions in violation of CGMP requirements.
Mckesson is recalling Dynarex DynaLube lubricating jelly due to facility temperature excursions from June-August 2021 that may have degraded product effectiveness. Recall affects 17.5 boxes distributed nationwide between June-September 2021.
Family Dollar Stores is recalling DRX Fiber Capsules (100 CT) distributed nationwide April 30–June 10, 2022, due to improper storage temperature conditions that violate good manufacturing practice requirements.
Family Dollar Stores is recalling MY CHOICE Levonorgestrel Tablets due to storage temperature deviations that may affect product efficacy. The tablets were distributed nationwide between April 30 and June 10, 2022.
Family Dollar Stores is recalling multiple deodorant and antiperspirant products because they were stored outside appropriate temperature conditions. No illnesses or injuries have been reported.
Family Dollar Stores is recalling specific Blistex Lip Medex products (SKUs 906120 and 998852) distributed April to June 2022 due to storage outside proper temperature conditions during distribution.
McKesson is recalling Medline Centurion IV Securement Kits that were exposed to high temperatures during storage, which may have impacted product effectiveness. No illnesses have been reported.
Baxter Healthcare is recalling DISCPAC Syringe Tip Caps due to potential packaging defects that may not maintain sterile barriers. The recall affects approximately 63,190 units distributed worldwide.
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.
Multiple bismuth-based antacid products distributed by Family Dollar Stores are being recalled due to storage temperature deviations that violate manufacturing standards. No illnesses have been reported.
Family Dollar's Guardian Antacid products were held outside appropriate storage temperatures, prompting an FDA Class II recall. Consumers should stop using affected products.
Family Dollar Stores recalls Disney Licensed Anti Bac Wipes and Antibacterial Wipes due to storage temperature deviations. The products were distributed nationwide to Family Dollar stores from April 30 through June 10, 2022.
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.
Dulcolax 5 mg tablets distributed to Family Dollar Stores between April 30 and June 10, 2022 are recalled because they were stored outside appropriate temperature conditions, which could affect product effectiveness.
Family Dollar Stores is recalling Carmex lip balm products (three SKUs) distributed from April 30 to June 10, 2022, due to CGMP deviations involving improper storage temperature conditions.
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.
Materialise USA LLC is recalling ProPlan CMF Anatomical Model units where packages labeled MU22-INA-DUQ contained the wrong anatomical model inside. Recipients should verify their package contents match the label.
Family Dollar Stores is recalling QP Motion Sickness Tablet 8 CT (SKU 901583) packages distributed nationwide from April 30 to June 10, 2022, due to improper storage temperature conditions.
Dynarex lemon glycerin swabs distributed nationwide may have reduced effectiveness due to temperature excursions prior to delivery. All lots received between June 1 and September 30, 2021 are affected.
Three baby ointment products (Desitin Creamy, Baby Love, Desitin Maximum Strength) were recalled from Family Dollar Stores for being stored outside recommended temperature conditions. No illnesses or injuries have been reported.