cimzia (certolizumab pegol), 2x200mg/mL PREFILLED SYRINGES (2 single-dose), Rx ONLY, Manufactured by: UCB Inc., Smyrna, GA 30080, a) NDC 50474-710-79, b) Professional sample, NDC 50474-710-80; c) 3 cartons, STARTER KIT, NDC 50474-710-81.
UScimzia (certolizumab pegol), 2x200mg/mL PREFILLED SYRINGES (2 single-dose), Rx ONLY, Manufactured by: UCB Inc., Smyrna, GA 30080, a) NDC 50474-710-79, b) Professional sample, NDC 50474-710-80; c) 3 cartons, STARTER KIT, NDC 50474-710-81.
Recalling Firm: UCB Biosciences Inc.
Motif du rappel / Danger
TranslatedLack of Assurance of Sterility
Description du produit & Identification
Translatedcimzia (certolizumab pegol), 2x200mg/mL PREFILLED SYRINGES (2 single-dose), Rx ONLY, Manufactured by: UCB Inc., Smyrna, GA 30080, a) NDC 50474-710-79, b) Professional sample, NDC 50474-710-80; c) 3 cartons, STARTER KIT, NDC 50474-710-81.
Additional Source Details
| Field | Value |
|---|---|
| City | Smyrna |
| State | GA |
| Openfda › Nui › 1 | N0000175610 |
| Openfda › Nui › 2 | N0000175451 |
| Openfda › Unii | UMD07X179E |
| Openfda › Rxcui › 1 | 795081 |
| Openfda › Rxcui › 2 | 795085 |
| Openfda › Rxcui › 3 | 849597 |
| Openfda › Rxcui › 4 | 849599 |
| Openfda › Rxcui › 5 | 2724369 |
| Openfda › Rxcui › 6 | 2724370 |
| Openfda › Rxcui › 7 | 2724371 |
| Openfda › Rxcui › 8 | 2724372 |
| Openfda › Spl id | 4b984e6f-72ac-4fdc-e063-6394a90af105 |
| Openfda › Brand name | CIMZIA |
| Openfda › Spl set id | b4c2c9dc-a0bb-4d64-a667-a67ebe88392d |
| Openfda › Package ndc › 1 | 50474-700-62 |
| Openfda › Package ndc › 2 | 50474-700-61 |
| Openfda › Package ndc › 3 | 50474-710-79 |
| Openfda › Package ndc › 4 | 50474-710-80 |
| Openfda › Package ndc › 5 | 50474-710-81 |
| Openfda › Package ndc › 6 | 50474-750-10 |
| Openfda › Product ndc › 1 | 50474-700 |
| Openfda › Product ndc › 2 | 50474-710 |
| Openfda › Product ndc › 3 | 50474-750 |
| Openfda › Generic name | CERTOLIZUMAB PEGOL |
| Openfda › Product type | HUMAN PRESCRIPTION DRUG |
| Openfda › Pharm class epc | Tumor Necrosis Factor Blocker [EPC] |
| Openfda › Pharm class moa | Tumor Necrosis Factor Receptor Blocking Activity [MoA] |
| Openfda › Manufacturer name | UCB, Inc. |
| Openfda › Application number | BLA125160 |
| Openfda › Is original packager | true |
| Event id | 98915 |
| Address 1 | 1950 Lake Park Dr SE |
| Code info | Lot: CVZFW, Exp.:2026-JUL-04; CVZYG, Exp.: 2026-AUG-19; CWSYT, Exp.: 2026-OCT-22; CWDZY, Exp.:2026-NOV-20; CWTSD, Exp.:2026-DEC-11; CVTFK, Exp.:2026-JUL-04; CVTSN, Exp.: 2026-AUG-19; CWVGP. Exp.:2026-DEC-11; CVWXT, CVWXV, CVWXW, Exp.:2026-JUL-04; CWHFF, Exp.: 2026-OCT-22; CWNDS, Exp.: 2026-DEC-11. |
| Postal code | 30080-7648 |
| Report date | 20260527 |
| Product type | Drugs |
| Product quantity | 141,708 cartons |
| Reason for recall | Lack of Assurance of Sterility |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260508 |
| Initial firm notification | Letter |
| Center classification date | 20260520 |
Consumer Action Protocol: What You Should Do Immediately
Safety StepsInspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.
Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.
Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.
If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Drugs).
Your Legal Rights as a Consumer
Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.
Frequently Asked Questions About This Recall
FAQ GuideQ1:What should I do immediately if I own or bought cimzia (certolizumab pegol), 2x200mg/mL PREFILLED SYRINGES (2 single-dose), Rx ONLY, Manufactured by: UCB Inc., Smyrn...?
Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.
Q2:Can I get a full refund or free repair for this recall?
Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.
Q3:Do I need my original sales receipt to claim a remedy or refund?
In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.
Q4:Where can I verify official information for this safety alert?
This safety alert is aggregated directly from official regulatory agency records (FDA Drugs). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.
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Aperçu
- Entreprise responsableUCB Biosciences Inc.
- StatusOngoing
- Niveau de risqueClass II
- DistributionUS Nationwide.
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🚨 SAFETY ALERT: UCB Biosciences Inc. - cimzia (certolizumab pegol), 2x200mg/mL PREFILLED SYRINGES (2 single-dose), Rx ONLY, Manufactured by: UCB Inc., Smyrna, GA 30080, a) NDC 50474-710-79, b) Professional sample, NDC 50474-710-80; c) 3 cartons, STARTER KIT, NDC 50474-710-81. Check if your household is affected: https://therecallfile.com/fr/recalls/cimzia-certolizumab-pegol-2x200mg-ml-prefilled-syringes-2-single-dose/FDA-D-0546-2026
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