The Recall Desk

Hazard

Contamination Risk recalls

1,031 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all contamination risk recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

76–100 of 1031

  • HighFDA (Devices)·Z-0692-2026·2025-12-03

    IV Administration Sets recalled due to backflow and occlusion potential

    B. Braun Medical Inc is recalling 45,288 units of IV Administration Sets due to potential backflow of medication from secondary containers into primary containers and inability to prime, which could cause improper medication delivery or line contamination.

    Product
    IV Administration Set utilized in gravity IV administration sets and pump administration sets utilized with BBMI's Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Labeled as the following with corresponding catalog number: 1. 130 IN. IV ADMIN SET W/ 9 I
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0173-2026·2025-11-26

    PeriGuard Ointment Recalled for CGMP Deviation at Manufacturing Facility

    DermaRite Industries is recalling PeriGuard Ointment due to manufacturing practice violations at the facility where contamination was found in other products. Affected are 381,619 units distributed nationwide.

    Product
    PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC 61924-205-07) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0174-2026·2025-11-26

    Renew PeriProtect Topical Cream Recalled for Manufacturing Facility Deviation

    DermaRite Industries is recalling Renew PeriProtect topical cream due to current good manufacturing practice (CGMP) violations at the manufacturing facility, where other products were found contaminated.

    Product
    Renew PeriProtect, Zinc Oxide 12%, Dimethicone 1%, 113g (4 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-435-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0548-2026·2025-11-26

    Blood collection device recalled due to unvalidated manufacturing processes

    ASP Global is recalling 6,600 SAFE-T-FILL Micro Capillary Blood Collection devices due to manufacturing under an inadequate quality system with unvalidated processes. The devices were distributed nationwide in the US and Canada.

    Product
    SAFE-T-FILL Micro Capillary Blood Collection, 300 ¿L; Prepared with Clot Activator; Red Model/Catalog Number: 07 7151 Product Description: The SAFE-T-FILL Capillary Blood Collection System is a collection device used to draw capillary blood from the finger or heelstick.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0165-2026·2025-11-26

    DermaSarra Camphor External Analgesic Recalled Due to Manufacturing Defect

    DermaSarra Camphor 0.5% external analgesic is being recalled due to a manufacturing practice deviation at the production facility. The recall affects 2,389 bottles distributed nationwide.

    Product
    DermaSarra, Camphor 0.5%, External Analgesic, 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0171-2026·2025-11-26

    Skin Protectant with Lanolin Recalled for Manufacturing Facility Contamination

    Skin Protectant with Lanolin, manufactured by DermaRite Industries, is being recalled due to CGMP violations and contamination detected in other products at the same manufacturing facility. Nationwide distribution; 5,876 units affected.

    Product
    SKIN PROTECTANT WITH LANOLIN — SKIN PROTECTANT WITH LANOLIN (LANOLIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0483-2026·2025-11-19

    Olympus Electrosurgical Snares Recalled for Sterility Compromise

    Olympus Corporation recalls 18,174 electrosurgical snares due to sterility compromise from packaging defects. Small holes in device pouches may allow contamination of the surgical instruments.

    Product
    Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400 Product Name: Single Use Single Use Electrosurgical Snare Model/Catalog Number: SD-U400U-15 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0421-2026·2025-11-12

    MAHURKAR Triple Lumen Catheter Tray Recalled Due to Packaging Seal Issue

    Mozarc Medical is recalling 3,258 units of MAHURKAR Acute High Pressure Triple Lumen Catheter Trays due to a potential seal integrity issue in the header bag packaging.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 13 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0424-2026·2025-11-12

    MAHURKAR Catheter Tray Recalled for Header Bag Seal Integrity Issue

    Mozarc Medical is recalling MAHURKAR Acute High Pressure Triple Lumen Catheter Trays due to a potential seal integrity issue with the header bag packaging. The recall affects 3,258 units distributed nationwide.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0426-2026·2025-11-12

    MAHURKAR Catheter Tray Recalled for Potential Packaging Seal Integrity Issue

    Mozarc Medical US LLC recalls MAHURKAR acute high-pressure triple lumen catheter trays nationwide due to potential seal integrity defects in header bag packaging. The issue could compromise product sterility.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Safety Components: 12 Fr/Ch (4.0 mm) x 24 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0119-2026·2025-11-05

    Semaglutide Injection Recalled for Lack of Sterility Assurance

    ProRx LLC is recalling 2,805 vials of Semaglutide Injection (5 mg/2 mL) due to lack of assurance of sterility. The affected lot was distributed in Texas and Utah.

    Product
    Semaglutide Injection, 5 mg/2 mL (2.5 mg/mL), 2mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-02
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Drugs)·D-0120-2026·2025-11-05

    Tirzepatide Injection Recalled for Lack of Sterility Assurance

    ProRx LLC is recalling 2,761 vials of Tirzepatide Injection due to lack of assurance of sterility. The affected lot was distributed to Texas and Utah.

    Product
    Tirzepatide Injection, 27 mg/3 mL (9 mg/mL), 3mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-209-03
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Drugs)·D-0099-2026·2025-11-05

    HADLIMA Injectable Drug Recalled for Lack of Sterility Assurance

    HADLIMA (adalimumab-bwwd) injectable is being recalled due to lack of assurance of sterility. The recall affects 5,518 packs distributed to a single warehouse in New Jersey.

    Product
    HADLIMA (adalimumab-bwwd) injection, 40mg/0.8 mL, 2 Single-dose Prefilled Syringes per carton, Rx only, Manufactured for: Organon LLC, a subsidiary of ORGANON & Co, Jersey City, NJ 07302, Manufactured by: SAMSUN BIOEPIS Co., Ltd, Incheon, Republic of Korea, NDC 78206-183-01.
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-0306-2026·2025-11-05

    Alcon Surgical Accessory Devices Recalled for Incomplete Sterile Barrier Seals

    Alcon is recalling surgical accessory devices for Unity and Constellation consoles due to incomplete seals in sterilization pouches. The compromised seals may allow contamination during vitrectomy procedures.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065000393 UNITY HP VISCOUS FLUID CONTROL VFC PACK Software Version: N/A Product Descr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0305-2026·2025-11-05

    Alcon surgical console accessories recalled due to incomplete sterile seals

    Alcon Laboratories is recalling accessory devices for surgical consoles due to incomplete seals in sterile packaging. The sterile barrier may be compromised, potentially allowing contamination before use.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065750918 PAK,I/A LINE,NGVS 8065750957 ASSY,SHIP,CONSTELLATION VFC 8065750972 ENDOILLUM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0135-2026·2025-10-22

    C-Rex UNO Surgical Instrument Recalled for Sterile Packaging Compromise

    Iantrek Inc. is recalling C-Rex UNO Microinterventional Goniotomy Instruments (Model CRX-120) due to potential compromised sterile packaging. The recalled lot numbers are 351729 and 351759, distributed nationwide.

    Product
    C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120. Product Description: The C-Rex UNO Microinterventional Goniotomy Instrument is a sterile single use disposable manual surgical instrument used in ophthalmic procedures for ab interno goniotomy and inne
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0054-2026·2025-10-15

    GenoGenix Glycine for Injection Recalled for Lack of Sterility Assurance

    GenoGenix LLC is recalling all strengths of Glycine for Injection distributed nationwide due to lack of assurance of sterility. No illnesses have been reported.

    Product
    Glycine for Injection, all strengths and presentations, GenoGenix LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0065-2026·2025-10-15

    NAD+ Injectable Solution Recalled for Lack of Sterility Assurance

    GenoGenix LLC is recalling all NAD+ injectable solution vials due to lack of assurance of sterility. All affected lots within expiration remain available for return.

    Product
    NAD+ (Nicotinamide adenine dinucleotide), a) 50 mg/mL, b) 100 mg/mL, 10 mL multi-dose vials, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0053-2026·2025-10-15

    GenoGenix Glutathione Injection Recalled Over Sterility Concerns

    GenoGenix is recalling all lots of Glutathione Preserved for Injection nationwide due to lack of assurance of sterility. Non-sterile injectable products could expose patients to serious infections.

    Product
    Glutathione Preserved for Injection, all strengths and presentations, GenoGenix LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0073-2026·2025-10-15

    EDTA for Injection Recalled Due to Sterility Assurance Defect

    GenoGenix LLC is recalling all lots of EDTA for Injection nationwide due to lack of assurance of sterility, affecting all strengths and presentations.

    Product
    EDTA for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0043-2026·2025-10-15

    B12 Methylcobalamin Injectable Recalled Due to Lack of Sterility Assurance

    GenoGenix LLC is recalling all strengths of B12 Methylcobalamin for Injection nationwide due to lack of assurance of sterility. All lots within expiry are affected.

    Product
    B12 Methylcobalamin for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as, manufactured for Synergy Wellness.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0060-2026·2025-10-15

    Lipo MIC +B12 Methylcobalamin Injection Recalled Over Sterility

    GenoGenix LLC is recalling Lipo MIC +B12 Methylcobalamin for Injection nationwide due to lack of assurance of sterility. Consumers should discontinue use and contact their healthcare provider.

    Product
    Lipo MIC +B12 Methylcobalamin for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0082-2026·2025-10-15

    Sterile Saline Reconstitution Solution Recalled Due to Lack of Sterility Assurance

    GenoGenix LLC is recalling all lots of Sterile Saline Reconstitution Solution for Injection nationwide due to lack of sterility assurance. No illnesses or injuries have been reported.

    Product
    Sterile Saline Reconstitution Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0068-2026·2025-10-15

    Ultra Burn for Injection Recalled for Sterility Assurance Failure

    GenoGenix is recalling all lots of Ultra Burn for Injection due to lack of assurance of sterility. Patients using this product should contact their healthcare provider.

    Product
    Ultra Burn for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0081-2026·2025-10-15

    Reconstitution XO Solution for Injection Recalled Due to Sterility Concerns

    Reconstitution XO Solution for Injection is being recalled nationwide due to lack of assurance of sterility in the manufacturing process.

    Product
    Reconstitution XO Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health a) 5% Exosomes, 10 mL vial and b) 10% Exosomes, 5 mL vial, Extension Health a) 20% Exosomes,
    Category
    Drug
    Distribution
    Distributed nationwide