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Lower risk Drug recall · FDA · Published January 26, 2022

Cardinal Healthcare Enoxaparin Syringes Recall: Temperature Exposure Risk

Cardinal Healthcare recalls 150mg/ml enoxaparin syringes due to potential temperature exposure during storage. This may affect product stability and safety.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0179-2024DrugCardinal Healthcare ›
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Recalling firmCARDINAL HEALTHCARE7200 Cardinal Pl W · Dublin, OH 43017-1094
✎ GovInfoNow plain-language explainer

What happened, in plain English

Cardinal Healthcare is recalling enoxap: 150mg/ml single-dose syringes with automatic safety device. The recall is because these syringes may have been exposed to temperatures outside the labeled storage conditions, which could affect product stability and safety. Read more at govinfonow.com/recall/35248-cardinal-healthcare-enoxaparin-syringes-recall-temperature-exposure-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/35248-cardinal-healthcare-enoxaparin-syringes-recall-temperature-exposure-risk · Updated August 18, 2026 · FDA enforcement record: FDA #D-0179-2024

Cite this page

“Cardinal Healthcare Enoxaparin Syringes Recall: Temperature Exposure Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35248-cardinal-healthcare-enoxaparin-syringes-recall-temperature-exposure-risk. Based on FDA recall #D-0179-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0179-2024%22&limit=1).

Why it’s dangerous

The syringes were exposed to temperatures outside the labeled storage conditions during manufacturing. This could potentially affect the product's stability and safety, though the risk is not severe enough to cause serious injury in normal use.

Who’s affected

Patients prescribed enoxaparin injections and healthcare providers using these syringes are likely affected. Those who have the specific batch numbers and storage conditions may be at higher risk.

How to tell if you have this one

Check for the product name: Enoxaparin Sodium Injection, USP, 150MG/ML Single-Dose Syringes with Automatic Safety Device. Look for the batch number SAH06821A on the packaging.

  • Brand
    Cardinal Healthcare
  • Category
    Drug
FDA recall event · 42 products

All 42 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationwide USA
Recall numberProduct, codes & lotsQuantityNDC
D-0161-2024Ipratropium Bromide and Albuterol Sulfate Inhalation Solution (0.5 mg/3 mg per 3 mL), 60 x 3 mL Sterile Unit-Dose Vials (2 pouches of 30 - 3 mL vials each), Manufactured By: The Ritedose Corporation, Columbia, SC 29203; Distributed By: Cipla USA Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-840-64; Batch 21C562 cartons69097-840-34, 69097-840-53, 69097-840-87, 69097-840-64
D-0162-2024ALBUTEROL SULFATE HFA Inhalation Aerosol, 90MCG per actuation, 200 Metered Inhalations, Net Wt. 18 g, Rx Only, Manufactured for: Prasco Laboratories, Mason, OH 45040 USA. NDC: 66993-019-68; Batch MY7E2 cartons66993-019-68
D-0163-2024ALBUTEROL SULFATE IN 90MCG per actuation, 200 Metered Inhalations, Rx Only, 8.5 g Net Contents, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Pithampur (M.P.) 454 775, India. NDC: 68180-963-01; Batch K10071511 cartons68180-963-01
D-0164-2024ALLOPURINOL Tablets, USP 300 MG 500 count Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106. NDC: 55111-730-05; Batch L1008131 unit55111-729-01, 55111-729-10, 55111-730-01, 55111-730-05
D-0165-2024AMOXICILLIN for Oral Suspension USP, 400MG/5ML, 100ML (when reconstituted), Manufactured In Canada By: TEVA CANA LIMITED, Toronto, Canada M1B 2K9; Manufactured For: TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454. NDC: 0093-4161-73; Batch 35447184A3 units0093-2263-01, 0093-2264-01, 0093-4160-76, 0093-4160-78, 0093-4160-73, 0093-4155-79, 0093-4155-73, 0093-4155-80, 0093-4161-76, 0093-4161-78, 0093-4161-73, 0093-2267-01, 0093-2268-01, 0093-3107-01, 0093-3107-05, 0093-3109-53, 0093-3109-05
D-0166-2024AMOXICILLIN Tablets, USP, 875MG, 20 Tablets, Rx Only, Manufactured by Sandoz GmbH for Sandoz Inc., Princeton, NJ 08540. NDC: 0781-5060-20; Batch LJ90042 units0781-2020-31, 0781-2020-76, 0781-2020-01, 0781-2020-05, 0781-2613-31, 0781-2613-76, 0781-2613-01, 0781-2613-05, 0781-5060-20, 0781-5060-01, 0781-5061-20, 0781-5061-01, 0781-6039-58, 0781-6039-46, 0781-6039-55, 0781-6156-52, 0781-6156-57, 0781-6156-46, 0781-6041-58, 0781-6041-46, 0781-6041-55, 0781-6157-52, 0781-6157-57, 0781-6157-46
D-0167-2024Aripiprazole Tablets, USP, 5 mg, 30 Tablets per bottle, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC: 65162-897-03; Batch AR2023182 units65162-896-03, 65162-896-09, 65162-896-50, 65162-896-11, 65162-897-03, 65162-897-09, 65162-897-50, 65162-897-11, 65162-898-03, 65162-898-09, 65162-898-50, 65162-898-11, 65162-899-03, 65162-899-09, 65162-899-50, 65162-899-11, 65162-901-03, 65162-901-09, 65162-901-50, 65162-901-11, 65162-902-03, 65162-902-09, 65162-902-50, 65162-902-11
D-0168-2024ARMOUR THYROID (thyroid tablets, USP), 2 GRAIN (120 mg), 100 Tablets, Rx Only, Distributed by: Allergan US, INc., Madison, NJ 07940. NDC: 0456-0461-01; Batch W055431 unit0456-0457-01, 0456-1045-01, 0456-0458-01, 0456-0458-11, 0456-0458-63, 0456-0459-01, 0456-0459-11, 0456-0459-63, 0456-0460-01, 0456-0461-01, 0456-0461-11, 0456-0461-63, 0456-0462-01, 0456-0463-01, 0456-0464-01
D-0169-2024Asmanex Twisthaler (mometasone furoate inhalation powder, 220 mcg per actuation), 120 Metered Doses, Rx only, Manufactured for: Organon LLC, a subsidiary of Organon & Co., Jersey City, NJ 07302; Manufactured by: MSD International GmbH (Singapore Branch) Singapore 638030, Singapore. NDC: 78206-114-01; Batch U0274583 units78206-114-03, 78206-114-04, 78206-114-02, 78206-114-01, 78206-114-59, 78206-115-59, 78206-115-01
D-0170-2024Low Dose ASPIRIN, 81 mg, 120 Enteric Coated Tablets, Distributed by: Rugby Lavoratories, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1234-41; Batch P1262012 units0536-1234-41
D-0171-2024Bumetanide Tablets, USP, 2 mg, 100 Tablets per bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382213 India; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807; Batch AM2111711 unit—
D-0172-2024CHLORTHALIDONE Tablets, USP, 25MG, 1000 Tablets, Rx only, Manufactured by: Appco Pharma LLC, Piscataway, NJ 08854 USA; Manufactured For: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA. NDC: 43598-719-10; Batch 2107329UM1 unit43598-719-01, 43598-719-10, 43598-720-01, 43598-720-10
D-0173-2024CITALOPRAM Tablets, USP, 20MG, 100 Tablets, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 0378-6232-01; Batch 31317481 unit0378-6231-01, 0378-6231-05, 0378-6232-01, 0378-6232-05, 0378-6233-01, 0378-6233-05
D-0174-2024Colgate Total SF Toothpaste, Net Wt 4.8 oz (136 g), Stannous Fluoride 0.454%, Clean Mint, Dist. by: COLGATE-PALMOLIVE CO., New York, NY 10022 USA; Batch 1293US561C1 unit—
D-0175-2024Dicyclomine Hydrochloride Tablets, USP 20 mg, 100 Tablets, Rx only, Manufactured For: Teva Pharmaceuticals USA, Parsippany, NJ 07054. NDC: 0591-0795-01; Batch 31977901 unit0591-0794-01, 0591-0794-10, 0591-0795-01, 0591-0795-10
D-0176-2024Donepezil HCl Tablets, 10 mg, 90 Tablets, Rx only, Distributed by: Solco Healthcare U.S. LLC, Hurracao, Puerto Rico 00791. NDC: 43547-276-09; Batch 176161 unit43547-275-03, 43547-275-09, 43547-275-11, 43547-276-03, 43547-276-09, 43547-276-11
D-0177-2024Donepezil HCl Tablets, 5 mg, 90 Tablets, Rx only, Distributed by: Solco Healthcare U.S. LLC, Hurracao, Puerto Rico 00791. NDC: 43547-275-09; Batch 176051 unit43547-275-03, 43547-275-09, 43547-275-11, 43547-276-03, 43547-276-09, 43547-276-11
D-0178-2024Doxycycline Capsules, USP 100 mg, 50 Capsules, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202 Unite States; Manufactured by: Lupin Limited, Nagpur - 441 108, INDIA. NDC 68180-652-08; Batch G1048191 unit68180-650-01, 68180-651-01, 68180-652-29, 68180-652-08
D-0179-2024Enoxaparin Sodium Injection, USP, 150MG/ML Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Ten 1 mL Syringes per box, Rx Only, Sandoz Inc, Princeton, NJ 08540. NDC: 0781-3299-69; Batch SAH06821A2 units0781-3238-01, 0781-3238-63, 0781-3246-02, 0781-3246-64, 0781-3256-03, 0781-3256-66, 0781-3262-04, 0781-3262-68, 0781-3268-05, 0781-3268-69, 0781-3298-04, 0781-3298-68, 0781-3299-05, 0781-3299-69
D-0180-2024ESTRADIOL TABLETS USP, 0.5MG 100 Tablets, Tx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454. NDC: 0555-0899-02; Batch 1000236871 unit0555-0899-02, 0555-0886-02, 0555-0886-04, 0555-0887-02, 0555-0887-04
D-0181-2024FIRST LANSOPRAZOLE PT 3MG/ML, 300ML, Rx Only, Distributed By: CutisPharma, Inc., Woburn, MA 01801. NDC: 65628-080-10; Batch 21025A1 unit—
D-0182-2024Fluticasone Propionate Nasal Spray USP, 50MCG per spray, 16 g net fill weight, 120 Metered Sprays, For Intranasal Use Only, Rx Only, Manufactured for: Apotext Corp., Weston, FL 33326. NDC: 60505-0829-1; Batch TE9159, TE81566 units60505-0829-1
D-0183-2024FOLIC ACID TABLETS, USP, 1MG, 100 Tablets per bottle, Rx Only, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004. NDC: 69315-127-10; Batch H082211 unit69315-127-01, 69315-127-10
D-0184-2024HydrALAZINE Hydrochloride Tablets, USP, 25 mg, 100 Tablets per bottle, Rx only, Distributed by: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816. NDC: 23155-002-01; Batch G210553, G2105512 units23155-001-01, 23155-001-10, 23155-002-10, 23155-002-01, 23155-003-01, 23155-003-10, 23155-004-01, 23155-004-10
D-0185-2024Jardiance (empagliflozin tablets), 25 mg, 30 tablets (3 blister cards with 10 tablets each), Rx only, Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877. NDC: 0597-0153-37; Batch D419191 unit0597-0152-90, 0597-0152-07, 0597-0152-70, 0597-0152-37, 0597-0152-30, 0597-0153-37, 0597-0153-30, 0597-0153-90, 0597-0153-07, 0597-0153-70
D-0186-2024Leader Nasal Decongestant PE (Phenylephrine HCl 10 mg), 18 Tablets per cartons, Distributed By Cardinal Health, Dublin, Ohio 43017. NDC: 70000-0126-1; Batch P1255141 unit—
D-0187-2024Lillow (Levonorgestrel and Ethinyl Estradiol Tablets, USP), 0.15 mg/0.03 mg, 1 Blister Pack Containing 28 Tablets, Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC 69238-1554-6; Batch A59211 unit—
D-0188-2024Lisinopril and Hydrochlorothiazide Tablets USP, 10mg/12.5mg, Rx only, 100 Tablets per bottles, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Nagpur-441 108, India. NDC: 68180-518-01; Batch Q101699, Q1019812 units68180-518-02, 68180-518-01, 68180-518-30, 68180-519-30, 68180-519-01, 68180-519-02, 68180-520-02, 68180-520-30, 68180-520-01
D-0189-2024Lithium Carbonate Extended-Release Tablets, USP, 300 mg, 100 Tablets per bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. NDC: 0378-1300-01; Batch 31383261 unit—
D-0190-2024Meloxicam Tablets, USP, 15 mg, 1000 Tablets per bottle, Rx Only, Manufactured by: Cipla Ltd., Kurkumbh, India; Manufactured for: Cipla USA, Inc., 9100 S. Dadeland Blvd., Suite 1500 Miami, FL 33156. NDC: 69097-159-15; Batch KA114891 unit69097-158-15, 69097-158-07, 69097-158-12, 69097-159-12, 69097-159-07, 69097-159-15
D-0191-2024Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, 1000 Tablets, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454. NDC: 45963-676-96; Batch 2447J2111 unit45963-709-11, 45963-709-96, 45963-676-11, 45963-676-96, 45963-677-11, 45963-677-96, 45963-678-11
D-0192-2024Nyamyc, 100,000 USP units per gram, 60 grams, Rx only, Topical Use Only, Manufactured by: Upsher-Smith Laboratories, Inc, Minneapolis, MN 55447.; Batch 4004542 units—
D-0193-2024PredniSONE Tablets, USP, 20 mg, 100 Tablets per bottle, Rx Only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801. NDC: 59746-175-06; Batch 21P06591 unit—
D-0194-2024Propranolol Hydrochloride Tablets, 20 mg, 100 Tablets per bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382213, India; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC: 69238-2078-1; Batch 1000235962 units69238-2077-1, 69238-2077-7, 69238-2078-1, 69238-2078-7, 69238-2079-1, 69238-2079-7, 69238-2080-1, 69238-2081-1, 69238-2081-5
D-0195-2024Ricola CherryHoney Herb Throat Drops (menthol, 1.8 mg), 10 Drops per roll, Manufacturer: Ricola Ltd., 4242 Laufen, Switzerland; Distributed by: Ricola USA Inc., 6 Campus Drive, 2nd Floor South, Parsippany, NJ 07054. NDC: 54305-507-10; Batch 20000586932 units54305-507-10, 2000058693
D-0196-2024RIVASTIGMINE TRANSDERMAL SYSTEM, Delivers 4.6 mg/24 hours, 30 systems per box, Rx Only, Distributed by: Alvogen, Inc., Morristown, NJ 07960. NDC 47781-304-03; Batch P0248AL0AT1 unit—
D-0197-2024SPIRIVA HANDIHALER (tiotropium bromide inhalation powder) 18 mcg/Capsule, 30 capsules, 3 blister cards, each card contains 10 capsules, Rx only, For oral inhalation only, Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877 USA. NDC: 0597-0075-41; Batch 1044405 units0597-0075-41, 0597-0075-75, 0597-0075-47
D-0198-2024Terconazole Vaginal Suppositories, 80 mg, 3 Suppositories with Vaginal Applicator, Rx only, Manufactured by: Cosette Pharmaceuticals, Inc., 111 Coolidge Street, South Plainfield, NJ 07080. NDC: 0713-0552-73; Batch 1014228A1 unit0713-0552-73
D-0199-2024Triamterene and Hydrochlorothiazide Capsules, USP, 37.5 mg/25 mg, 100 capsules per bottle, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 19136. NDC 0527-1632-01; Batch 21000279A, 21000280A2 units—
D-0200-2024Warfarin Sodium Tablets, USP, 2.5 mg, 100 Tablets per bottle, Rx only, Manufactured For: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC: 0093-1714-01; Batch 21690411 unit0093-1712-01, 0093-1712-10, 0093-1713-01, 0093-1713-10, 0093-1714-01, 0093-1714-10, 0093-1715-01, 0093-1716-01, 0093-1716-10, 0093-1721-01, 0093-1721-10, 0093-1718-01, 0093-1723-01, 0093-1720-01
D-0201-2024Warfarin Sodium Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC: 0093-1721-01; Batch 23230411 unit0093-1712-01, 0093-1712-10, 0093-1713-01, 0093-1713-10, 0093-1714-01, 0093-1714-10, 0093-1715-01, 0093-1716-01, 0093-1716-10, 0093-1721-01, 0093-1721-10, 0093-1718-01, 0093-1723-01, 0093-1720-01
D-0202-2024Inhub Wixela (fluticasone propionate and salmeterol inhalation powder, USP) 500/50MCG, 60 Doses of Inhalation Powder, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. NDC: 0378-9320-32; Batch 620025321 unit0378-9320-32, 0378-9321-32, 0378-9322-32
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the batch number on the syringe packaging; the affected batch is SAH06821A.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.7 years after the firm started it.

1. Firm started the recall: Jan 26, 202212. FDA classified it Class II: Dec 26, 202323. Published in FDA’s Enforcement Report: Jan 3, 202434. FDA terminated the recall: Sep 29, 2024420222024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Keep exploring

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0179-2024 (January 26, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0179-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA