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.

9301–9325 of 21595

  • ModerateFDA (Food)·F-1157-2019·2019-03-20

    Kradjian Importing Recalls Zarrin Pickled Cucumbers Due to Leaking Cans

    Kradjian Importing Co is recalling Zarrin Pickled Cucumbers & Cornichons because some cans are leaking and swollen. Consumers should stop using the product.

    Product
    Zarrin Pickled Cucumbers & Cornichons: Net Weight 101.4 oz. 3 kg. Ingredients: Cucumber, water, salt, acid (acetic acid, spices, food coloring (tartrazine). Refrigerate after opening. UPC 7 64363 18305 2 Product of the West Bank Packed for Blanish International, PO Box 2
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1009-2019·2019-03-20

    Olympus PCF-Q180AC Video Colonoscope Recalled Due to Adhesive Error

    Olympus is recalling two video colonoscopes because the adhesive used in their repair was incorrectly prepared, potentially affecting the durability of the repair.

    Product
    Olympus PCF-Q180AC Video Colonoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1005-2019·2019-03-20

    Zimmer NexGen Trabecular Metal Tibial Augment Recall for Label Mismatch

    Zimmer Trabecular Metal Technology is recalling 24 units of NexGen Tibial Half Block Augments because the product in the box may not match the label.

    Product
    NexGenTrabecular Metal Tibial Half Block Augment, Right Lateral/Left Medial, Size 4 5MM Thickness W/Screws Item Number: 00544800426 Product Usage: The Trabecular Metal Tibial Cone Augments are intended for use where severe degeneration, trauma, or other pathology of the kne
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1003-2019·2019-03-20

    Ossur ReSolve Halo Vest Recalled for Labeling and Safety Testing Issues

    Ossur Americas is recalling 381 ReSolve Halo Vests because the titanium pin label incorrectly lists a ceramic tip and the products require confirmatory safety testing.

    Product
    Ossur, ReSolve Halo Vest, Part/ Description: 545700K/ ReSolve Halo Vest-shrt kodel; 545700L/ ReSolve Halo Vest-shrt lmbwool; 545800K/ ReSolve Halo Vest-tall kodel; 545800L/ ReSolve Halo Vest-tall lmbwool
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-0997-2019·2019-03-20

    Ossur Skull Pin Recall Due to Labeling Error and Safety Testing

    Ossur Americas is recalling 372 sterile titanium skull pins because the label incorrectly lists a ceramic tip and the products require confirmatory safety testing.

    Product
    Ossur Skull Pin, Sterile Titanium Pin, Part/Description: 516TS/ Skull Pin 2-1/4in TI Sterl 1PK; 516V2S/ Skull Pin 3in TI Sterl 1PK; 520TS/ Skull Pin 2-1/4in TI Sterl 5PK; 520V2S/ Skull Pin 3in TI Sterl 5 PK
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1007-2019·2019-03-20

    Olympus Ultrasound Gastrovideoscope Recalled Due to Adhesive Preparation Error

    Olympus is recalling one ultrasound gastrovideoscope because the adhesive used for its repair was incorrectly prepared, potentially affecting the device's durability.

    Product
    Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1008-2019·2019-03-20

    Olympus GIF-H180J Gastrointestinal Videoscope Recalled Due to Adhesive Error

    Olympus is recalling one GIF-H180J videoscope because the adhesive used for its repair was incorrectly prepared, potentially affecting the device's durability.

    Product
    Olympus GIF-H180J Gastrointestinal Videoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0999-2019·2019-03-20

    Ossur OB Resolve Sterile Ring Kits Recalled for Labeling Errors

    Ossur Americas is recalling 342 units of OB Resolve sterile ring kits due to a labeling error on titanium pins and pending safety testing.

    Product
    Ossur OB Resolve, Sterile, Part/ Description: 505300D/ OB RESOLVE STERILE RING SML; 505400D/ OB RESOLVE RING KIT STD; 505500D/ OB RESOLVE RING KIT LRG; 515300D/ OB RESOLVE RING KIT SM-No App; 515400D/ OB RESOLVE RING KIT STD-No App; 515500D/ OB RESOLVE RING KIT LG-No Ap
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Food)·F-1220-2019·2019-03-20

    JOY Coriander Chutney Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling specific sizes of Coriander Chutney because the product contains undeclared sulfites.

    Product
    JOY Coriander Chutney NET WT 8 OZ (228g), UPC:6 80617 60402 2 and NET WT 26 OZ (737g), UPC: 6 80617 60401 5
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-1003-2019·2019-03-20

    Macleods Pharma Recalls Telmisartan and Hydrochlorothiazide Tablets for Blend Uniformity

    Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed blend uniformity specifications.

    Product
    Telmisartan and Hyrdochlorothiazide Tablets 40mg/12.5 mg, 30-count bottles, Rx Only, Manufactured for:Macleods Pharma USA, Inc. Plainsboro, NJ 08536, Manufactured for: Macleods Pharmaceuticals Ltd. Baddi, Himchal Pradesh INDIA, NDC 33342-128-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1219-2019·2019-03-20

    JOY Chat Chutney Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling JOY Chat Chutney because it contains undeclared sulfites. The product was distributed in Connecticut, New York, and New Jersey.

    Product
    JOY Chat Chutney NET WT 8 OZ (228g), UPC:6 80617 60408 4
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1001-2019·2019-03-20

    Ossur Halo System Ring Kits Recalled for Labeling and Safety Testing

    Ossur Americas is recalling 182 units of Halo system ring kits due to a labeling error and the need for confirmatory safety testing.

    Product
    Ossur, Sterile, Part/ Description: 505300T/ CB RING KIT TI SM; 505300V2/ OB V2 RING KIT TI SM; 505400T/ CB RING KIT TI STD; 505400V2/ OB V2 RING KIT TI STD; 505500T/ CB RING KIT TI LG; 505500V2/ OB V2 RING KIT TI LG; 515300V2/ OB V2 RING KIT TI SM-No App; 515400V2/ OB
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1004-2019·2019-03-20

    Ossur LIL Angel Vest Recalled for Labeling and Safety Testing Issues

    Ossur Americas is recalling 45 LIL Angel Vests because the titanium pin labels incorrectly list ceramic tips and require confirmatory safety testing.

    Product
    Ossur, LIL Angel Vest, Part/ Description: 545100K/ LIL ANGEL VEST P2 KODEL; 545100L/ LIL ANGEL VEST P2 LAMBSWOOL; 545100S/ LIL ANGEL VEST P2 SORBATEX; 545150K/ LIL ANGEL VEST P3 KODEL; 545150L/ LIL ANGEL VEST P3 LAMBSWOOL; 545150S/ LIL ANGEL VEST P3 SORBATEX
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-0998-2019·2019-03-20

    Ossur Skull Pin Recall for Labeling Error and Safety Testing

    Ossur Americas is recalling 824 sterile skull pins due to a label error and pending safety testing.

    Product
    Ossur Skull Pin, Sterile Ceramic Tip Pin, Part/ Description: 516CS/ Skull Pin 2-1/4in CT Sterl 1PK; 516DS/ Skull Pin 3in CT Sterl 1PK; 517CS/ Skull Pin 2-1/4in CT Sterl 4PK; 517DS/ Skull Pin 3in CT Sterl 4 PK; 522CS/ Skull Pin 2-1/4in CT Sterl 6PK; 522C/ SKULL PIN 2-1/4
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Drugs)·D-1005-2019·2019-03-20

    Macleods Pharma Recalls Telmisartan and Hydrochlorothiazide Tablets for Blend Uniformity

    Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed content uniformity specifications for blend uniformity.

    Product
    Telmisartan and Hyrdochlorothiazide Tablets 80 mg/25 mg, 30-count bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals Ltd. Baddi Himachal Pradesh, INDIA, NDC 33342-130-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1213-2019·2019-03-20

    JOY Ginger Paste Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling JOY Ginger Paste in 8 oz and 26 oz sizes because the product contains undeclared sulfites.

    Product
    JOY Ginger Paste NET WT 26 OZ (737g), UPC: 6 80617 60001 7 and NET WT 8 OZ (228g), UPC: 6 80617 60002 4
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0979-2019·2019-03-20

    Cook Transseptal Needle Recalled for Missing Back Bevel

    Cook Inc. is recalling 100 units of Transseptal Needles manufactured without a back bevel on the needle tip, which could damage the introducer during insertion.

    Product
    Cook Transseptal Needle, Reference Number TSNC-18-71.0, Order Number G02364. For transseptal left heart access in both diagnostic and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1158-2019·2019-03-20

    Kradjian Imports Recalls Leaking and Swollen Bulgarian White Brined Sheep's Milk Cheese

    Kradjian Imports Co. is recalling 952 cases of Bulgarian White Brined Sheep's Milk cheese due to leaking and swollen cans. The product was distributed across 14 states.

    Product
    Bulgarian White Brined Sheep's Milk cheese; 5 gallon can Ingredients: Pasteurized Sheep's Milk, Bacterial culture, salt, rennet. Product of Belgium. Imported by Kradjian Imports Co., Inc., Glendale, CA 91204
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Food)·F-1214-2019·2019-03-20

    JOY Garlic Paste Recalled for Undeclared Sulfites

    JOY Gourmet Foods LLC is recalling specific jars of garlic paste because they contain undeclared sulfites. Consumers in Connecticut, New York, and New Jersey should check their pantries.

    Product
    JOY Garlic Paste NET WT 26 OZ (737 g) UPC: 6 80617 60003 1 and NET WT 8 OZ (228g) UPC: 6 80617 60004 8
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-1012-2019·2019-03-20

    Medtech Recalls Little Remedies New Baby Essentials Kit for Labeling Errors

    Medtech Products is recalling 4,716 Little Remedies New Baby Essentials Kits because the cartons contain incorrect labeling for two of the five items inside.

    Product
    Little Remedies New Baby Essentials Kit. Each kit contains 1 each of the following products: Little Remedies Infant Fever Reducer (acetaminophen 150mg) 2 fl. oz. bottle, Little Remedies Saline Spray/Drops (sodium chloride) 0.5 fl oz., Little Remedies Gripe Water (zingiber officin
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1004-2019·2019-03-20

    Macleods Pharma Recalls Telmisartan and Hydrochlorothiazide Tablets for Blend Uniformity

    Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed blend uniformity specifications. The recall covers 140,589 bottles distributed nationwide.

    Product
    Telmisartan and Hyrdochlorothiazide Tablets, USP 80mg/12.5 mg, 30-coun bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Imachal Pradesh, India NDC 33342-129-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1000-2019·2019-03-20

    Ossur CB Resolve Halo System Recalled for Labeling and Testing Issues

    Ossur Americas is recalling 656 units of CB Resolve Halo system products due to a labeling error and the need for confirmatory safety testing.

    Product
    Ossur CB Resolve, Sterile, Part/ Description: 505300C/ CB RESOLVE STERILE UNIT SML; 505400C/ CB RESOLVE STERILE UNIT STD; 505500C/ CB Resolve Sterile Unit LRG; 515300C/ CB RESOLVE RING KIT SM-No App; 515400C/ CB RESOLVE RING KIT STD-No App; 515500C/ CB RESOLVE RING KIT
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1002-2019·2019-03-20

    Ossur J Tong Sterile Medical Device Recall for Labeling Error

    Ossur Americas is recalling 138 units of J Tong sterile medical devices because the titanium pin label incorrectly lists a ceramic tip.

    Product
    Ossur, J Tong, Sterile, Part/ Description: JT-115/ J TONG MED/LGE-No App; JT-200/ J TONG ASSEMBLY SML/MED; JT-210/ J TONG ONLY SML/MED; JT-400/ J TONG COMPONENT TRAY
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-1010-2019·2019-03-20

    Olympus TJF-Q180V Duodenoscope Recalled Due to Adhesive Preparation Error

    Olympus is recalling two TJF-Q180V duodenoscopes because the adhesive used in their repair was incorrectly prepared, potentially affecting the device's durability or effectiveness.

    Product
    Olympus TJF-Q180V Duodenoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide