Accueil/Tous les Rappels/FDA-Z-2273-2026
FDA DevicesClass II

Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050

Publié le: 10 juin 2026ID du rappel: Z-2273-2026Catégorie: Dispositifs MédicauxPays: États-Unis
US
Medical DeviceFDA DevicesUSUS

Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050

Recalling Firm: Covidien LLC

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Traduire l’alerteTranslate notice text, hazard warnings, and descriptions into any supported language.

Motif du rappel / Danger

Temperature probe devices lack FDA clearance.

Description du produit & Identification

Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050

Produits concernés

Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050

Additional Source Details

FieldValue
CityBoulder
StateCO
Event id98859
Address 16135 Gunbarrel Ave
Code infoUDI: 10884521828391, 30884521828395/ Lot: 24D1130JZX 25A1086JZX 25E1332JZX 25I1054JZX 24D1133JZX 25A1087JZX 25F0946JZX 25I1055JZX 24E1015JZX 25A1088JZX 25F0947JZX 25I1056JZX 24E1017JZX 25D0379JZX 25F0948JZX 25I1057JZX 24E1018JZX 25D0380JZX 25F0949JZX 25I1058JZX 24L0848JZX 25D0381JZX 25F0950JZX 25I1059JZX 24L0850JZX 25D1271JZX 25F0953JZX 25I1061JZX 25A1069JZX 25D1272JZX 25F0954JZX 25K1129JZX 25A1070JZX 25D1273JZX 25G1163JZX 25K1130JZX 25A1072JZX 25E1263JZX 25H0935JZX 25K1131JZX 25A1075JZX 25E1264JZX 25H0936JZX 25L0542JZX 25A1076JZX 25E1265JZX 25H0938JZX 25L0545JZX 25A1077JZX 25E1326JZX 25H0939JZX 25L0899JZX 25A1082JZX 25E1329JZX 25H0940JZX 25L0901JZX 25A1084JZX 25E1331JZX 25H0942JZX 25L0903JZX 25A1085JZX
Postal code80301-3214
Report date20260610
Product typeDevices
Product quantity128,900 units
Reason for recallTemperature probe devices lack FDA clearance.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260423
Initial firm notificationE-Mail
Center classification date20260529

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Inspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.

2Isolate & Discontinue Use

Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Devices).

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 Guide

Q1:What should I do immediately if I own or bought Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050?

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 Devices). 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 responsableCovidien LLC
  • StatusOngoing
  • Niveau de risqueClass II
  • DistributionUS Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IL, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, WA, WV.
Recall Hazard Severity
High Alert (Class I)
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🚨 SAFETY ALERT: Covidien LLC - Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050

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https://therecallfile.com/fr/recalls/covidien-mon-a-therm-general-purpose-temperature-probe-size-9-fr-ref-9/FDA-Z-2273-2026
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