The Recall Desk

Severity 2 of 5

Moderate recalls

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

What “moderate” means here

Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

2101–2125 of 3531

  • ModerateFDA (Devices)·Z-1800-2022·2022-10-05

    Wound Care Dressings Recalled Due to Temperature Exposure

    Mckesson is recalling Shur-Conform and ALGICELL wound care dressings due to temperature exposure affecting product effectiveness. All affected units were distributed June through September 2021.

    Product
    a. INTEGRA LIFESCIENCE (WND CARE) Shur-Conform Oil Emulsion Oil Emulsion Impregnated Dressing Shur-Conform 3 X 8 Inch Knitted Cellulose Acetate Petrolatum Emulsion Sterile Model Number: 77042. b. INTEGRA LIFESCIENCE (WND CARE) ALGICELL Ag Silver Alginate Dressing Algicell Ag
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1799-2022·2022-10-05

    Surgitube Surgical Bandages Recalled for Temperature Exposure During Storage

    McKesson is recalling Surgitube surgical bandages distributed between June and September 2021 that may have been exposed to elevated temperatures during storage. The FDA states the temperature exposure is unlikely to cause adverse health effects.

    Product
    a. DERMA SCIENCES, INC Surgitube BANDAGE, GAUZE SURGI WHT SZ15/8" 50YDS Catalog #GL-219. b. DERMA SCIENCES, INC Surgitube BANDAGE, GAUZE SURGI WHT SZ2 1" 50YDS Catalog # GL-220. c. DERMA SCIENCES, INC Surgitube BANDAGE, GAUZE SURGI WHT SZ4 25/8" 50YDS Catalog # GL-222. d. D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1542-2022·2022-10-05

    Ampicillin for Injection Recalled Due to Foreign Object Contamination

    Viatris Inc recalls 3,931 cartons of Ampicillin for Injection after a complaint of a hair strand found in one vial. No illnesses have been reported.

    Product
    Ampicillin for Injection, USP, 2 grams/vial NDC 67457-352-02, packaged in 10 x 2 g vials per carton NDC 67457-352-10, Rx only, Mylan Manufactured in India for: Mylan Institutional LLC Rockford, IL 61103 U.S.A
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1801-2022·2022-10-05

    Skin markers recalled due to storage temperature exposure

    Mckesson Medical-Surgical Inc. recalls skin markers used in medical imaging that may have been exposed to excessive temperatures during storage prior to delivery. Affected units were received between June and September 2021.

    Product
    Skin markers: a. IZI MEDICAL PRODUCTS LLC Multi-Modality Markers SKIN MARKER RADIO 1.5MM 50BX Catalog #MM3005. b. SKIN MARKER MAMMO BB2.0 100B - Mammography Skin Marker Catalog # SDM-BB20.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1787-2022·2022-10-05

    Saline wound flush recalled due to temperature exposure affecting effectiveness

    Mckesson is recalling SafeWash Saline Wound Flush due to temperature exposure that may have reduced product effectiveness. The recall affects units distributed nationwide from June through September 2021.

    Product
    DERMARITE INDUSTRIES SafeWash Saline Saline Wound Flush SafeWash 7.1 oz. Can Sterile 0.9% Sodium Chloride Model Number: 00245
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1807-2022·2022-10-05

    Wound Dressing Units Recalled Due to Storage Temperature Excursions

    KerraCel Ag wound dressing units distributed between June and September 2021 are being recalled due to facility temperature excursions that may have affected product effectiveness. The FDA states no adverse health consequences are likely.

    Product
    3M SYSTAGENIX/KCI KerraCel Ag DRESSING, WOUND KERRACEL AG 4X5 (10/CT 10CT/CS) Catalog #CWL1158
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateCPSC·22236·2022-09-29

    HyperJuice Stackable GaN USB-C Chargers Recalled for Fire Hazard

    Hyper Products is recalling about 18,200 HyperJuice Stackable GaN USB-C Chargers (models HJ414 65W and HJ417 100W) because they can overheat and pose a fire hazard. No injuries have been reported.

    Product
    HyperJuice Stackable GaN USB-C Chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1751-2022·2022-09-28

    Fruit blend products recalled for inadequate wash water sanitation

    Russ Davis Wholesale recalls Deluxe Fruit Blend and Deluxe Fruit Bowl products due to inadequate wash water sanitizer. Affected products were distributed to Iowa, Michigan, Minnesota, North Dakota, South Dakota, and Wisconsin.

    Product
    Deluxe Fruit Blend and Deluxe Fruit Bowl. Contains: Watermelon, Cantaloupe, Grapes, Pineapple, Blueberries, Strawberries. Packaged in the follow brands and sizes: 1. Item 80502. Net Wt. 14 oz. Crazy Fresh 2. Item 80504. Net Wt 10 oz. Crazy Fresh 3. Item 80861. Net W
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-1771-2022·2022-09-28

    Fruit Bowls Recalled Due to Inadequate Sanitizer in Wash Water

    Russ Davis Wholesale is recalling fruit bowls sold in six Midwestern states due to inadequate sanitizer in wash water used during processing. The recall affects approximately 87,915 units.

    Product
    Cantaloupe, Honeydew, Pineapple, Strawberries. Keep Refrigerated. Net Wt. 3 lbs. Packaged in the following brands 1. Item 81110. Sunrise Fruit Bowl. grocery store brands. 2. Item 81113. Fresh Fruit Value Bowl. Crazy Fresh, quick & easy, and grocery store brands.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1771-2022·2022-09-28

    Diversatek M-Catch Retrieval Nets: incorrect inner polybag labeling

    Diversatek Healthcare is recalling M-Catch Retrieval Nets (Part Number REF 1175-01, Lot Number 001919) due to incorrect inner polybag labeling. 245 devices were distributed nationwide between September and October 2021.

    Product
    Diversatek Health, M-Catch Retrieval Nets, Part Number REF 1175-01, Quantity 5 EA/u. Used to endoscopically retrieve severed polyps, tissue samples, food bolus, and foreign bodies in the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1777-2022·2022-09-28

    Summer Daze fruit salad recalled due to inadequate wash water sanitization

    Russ Davis Wholesale LLC is recalling Summer Daze fruit mixture products sold at Kowalski's Markets in the Midwest due to inadequate sanitizer used in wash water during processing.

    Product
    Summer Daze. Contains: Cantaloupe, Watermelon, Pineapple, Grapes, Blueberries. Keep Refrigerated. Packaged in the following brands and sizes: 1. Item 89270. Net Wt. 16 oz. Kowalski's Markets. 2. Item 89279. Net Wt. 40 oz. Kowalski's Markets.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-1753-2022·2022-09-28

    Strawberry, Kiwi, and Mango Products Recalled Due to Inadequate Sanitizer

    Russ Davis Wholesale is recalling strawberry, kiwi, and mango products sold under the Crazy Fresh and Strawberry Sunrise brands due to inadequate sanitizer in wash water. Products were distributed across six Midwestern states.

    Product
    Strawberry, Kiwi, Mango. Packaged in the following brands and sizes: 1. Item 80595. Net Wt. 14 oz. Crazy Fresh 2. Item 80866. Net Wt 20 oz. Crazy Fresh, quick & easy, and grocery store branded. 3. Item 89269. Strawberry Sunrise Net Wt. 16 oz. Kowalski's Markets 4.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-1738-2022·2022-09-28

    Mountain Dew Major Melon Zero 12-pack cans have incorrect sugar-content labeling

    Mountain Dew Major Melon Zero 12-pack cans sold nationwide are labeled 'Full Sugar' on the can despite containing Zero Sugar formula. The actual product is correct; only the can label is mislabeled.

    Product
    Mountain Dew Major Melon Zero, 12 FL OZ (355mL) can, sold as 12 pack. Bottled under the authority of Pepsico, Inc. Purchase, NY 10577. UPC 0 12000 20506 4 (can) UPC 0 12000 20507 1 (12 pack carton)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1763-2022·2022-09-28

    Four berry blend recalled due to inadequate wash water sanitization

    Russ Davis Wholesale is recalling 87,915 units of Four Berry Blend products distributed across the Midwest due to inadequate sanitizer in wash water.

    Product
    Four Berry Blend containing Strawberry, Blackberry, Blueberry, Raspberry. Keep Refrigerated. Item 80847. Net Wt. 12 oz. packaged in the following brands: .Crazy Fresh, quick & easy, and grocery store branded.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-1760-2022·2022-09-28

    Berry Tray Recall Due to Inadequate Sanitization

    Russ Davis Wholesale is recalling 87,915 units of Berry Tray with Fruit Dip due to inadequate sanitizer in wash water. Affected products were distributed in IA, MI, MN, ND, SD, and WI with best-by dates of 7/8–8/1/2022.

    Product
    Berry Tray with Fruit Dip containing Strawberry, Blackberry, Blueberry, raspberry and fruit dip. Net Wt. 1.5 lbs. Item 80822 Packaged under the following brands: Crazy Fresh, quick & easy, and grocery store branded.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-1541-2022·2022-09-28

    Clonidine Hydrochloride 0.3 mg Tablets Recalled for Strength Mix-up

    UNICHEM PHARMACEUTICALS is recalling Clonidine Hydrochloride Tablets labeled 0.3 mg that contain 0.2 mg tablets instead. The recall affects 18,960 bottles (Lot # GCLH22005) distributed nationwide.

    Product
    CLONIDINE HYDROCHLORIDE — CLONIDINE HYDROCHLORIDE (CLONIDINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1754-2022·2022-09-28

    Strawberry, Blueberry, and Blackberry Products Recalled for Inadequate Wash Sanitizer

    Russ Davis Wholesale is recalling strawberry, blueberry, and blackberry products sold under brands including Crazy Fresh and Kowalski's Markets due to inadequate sanitizer in wash water. Products with use-by dates of July 9 through August 2, 2022, are affected.

    Product
    Strawberry, Blueberry, and Blackberry packaged in the following brands and sizes: 1. Item 80610. Triple Berry Blend Net Wt. 14 oz. Crazy Fresh 2. Item 80867. Triple Berry Blend Net Wt 20 oz. Crazy Fresh, quick & easy, and grocery store branded. 3. Item 89272. Berry
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1774-2022·2022-09-28

    Fungitell STAT IVD Assay affected by incorrect printed reconstitution instructions

    Associates of Cape Cod is recalling Fungitell STAT IVD Assay kits due to incorrect printed information on clamshells regarding reconstitution and pretreatment volumes. Users should verify procedures against official documentation before use.

    Product
    Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum Ref: FT007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1770-2022·2022-09-28

    Dialysis water-treatment unit recalled for missing ferrite cores in cables

    Fresenius is recalling 6 units of the AquaC UNO H reverse osmosis unit used with hemodialysis systems due to missing ferrite cores in internal ethernet cables affecting electromagnetic compatibility.

    Product
    AquaC UNO H [120V, 60Hz, 1700VA, US-Version- a reverse osmosis unit intended for use with hemodialysis systems. Fresenius Part Number: 24-0970-1 Vivonic Part Number: G02000966-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1762-2022·2022-09-28

    Strawberry, Kiwi, and Blueberry Products Recalled for Inadequate Sanitization

    Russ Davis Wholesale is recalling strawberry, kiwi, and blueberry products distributed across the Midwest due to inadequate sanitizer in wash water. The recall affects 87,915 units sold under multiple retail brands.

    Product
    Strawberry, Kiwi, Blueberry packaged in the following sizes and brands: 1. Item 80846. Net Wt. 12 oz. Keep Refrigerated. Crazy Fresh, quick & easy, and grocery store branded. 2. Item 80865. Net Wt. 20 oz. Keep Refrigerated. Crazy Fresh, quick & easy, and grocery store
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-1765-2022·2022-09-28

    Deluxe Fruit Bowl recalled due to inadequate wash water sanitizer

    Russ Davis Wholesale is recalling Deluxe Fruit Bowl products (87,915 units) due to inadequate sanitizer in wash water. Affected products were distributed in six Midwestern states with use-by dates of July 26 to August 2, 2022.

    Product
    Deluxe Fruit Bowl. Contains Pineapple, Cantaloupe, Honeydew, Watermelon, Kiwi, Strawberry. Keep Refrigerated. Item 80935. Net Wt. 3.5 lb. Packed under brands: Crazy Fresh, quick & easy, and grocery store branded.
    Category
    Food
    Distribution
    6 states
  • ModerateCPSC·22228·2022-09-22

    Accompany USA Ceramic Mugs with Cork Bottoms Recall Due to Burn Hazard

    Accompany USA is recalling about 25,000 ceramic mugs with cork bottoms because they can crack or break when hot liquid is poured into them, posing a burn hazard. One incident of breakage has been reported with no injuries.

    Product
    Ceramic Mugs with Cork Bottoms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·22226·2022-09-22

    Miffy First LED Lights Recalled for Overheat Burn Hazard

    About 1,400 Miffy First LED Lights can overheat during use, posing a burn hazard. No injuries have been reported. Consumers should stop using the lights and contact the company for a free module replacement.

    Product
    Miffy First LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1741-2022·2022-09-21

    PTS Panels CHOL+GLU Test Strips Recalled for Incorrect Instructions

    PTS Panels CHOL+GLU Test Strips (lot A202) are recalled because incorrect instructions for use were packaged with the product. Distribution includes the US, Japan, and Russia.

    Product
    PTS Panels CHOL+GLU Test Strips (REF 1765)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1535-2022·2022-09-21

    Triamcinolone Acetonide Cream Recalled Due to Manufacturing Quality Defects

    Direct Rx is recalling Triamcinolone Acetonide cream 0.1% due to manufacturing quality deviations that resulted in gritty texture and lack of effectiveness. The affected lot is 12JY2216, expiring February 29, 2024.

    Product
    TRIAMCINOLONE ACETONIDE — TRIAMCINOLONE ACETONIDE (TRIAMCINOLONE ACETONIDE CREAM)
    Category
    Drug
    Distribution
    2 states