Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Mohnark Pharmaceuticals Inc., of Davie, Fla.

Mohnark Pharmaceuticals Inc., of Davie, Fla. Recalls

All product recalls associated with Mohnark Pharmaceuticals Inc., of Davie, Fla..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 5521–5540 of 25000 recalls

Lidocaine Cream (Mohnark) – child-resistant packaging (2022)

The recall involves Mohnark Pharmaceuticals Lidocaine 4% Topical Anesthetic Cream. The product was sold in a white tube with a flip-top closure. Mohnark Pharmaceuticals is printed under the blue and green logo on the right side of the product tube. The lot code is located at the bottom of the product tube. The affected lot codes are 01202201, 210201, 210301, 210503, 210505, 210601, 211002 and 210401. The UPC 860002324906 is located on bottom side panel of the packaging.

CPSCJun 30, 2022Nationwide• Mohnark Pharmaceuticals Inc., of Davie, Fla.

Testosterone Gel 1% (Teva) – Superpotent Drug Issue (2022)

Superpotent Drug: Out of specification assay result was obtained during stability testing.

Class IIModerate

FDAJun 29, 2022Nationwide• Teva Pharmaceuticals USA Inc

Telmisartan Hydrochlorothiazide Tablets (Glenmark) – Packaging Issue (2022)

1...275 276277278 279...1250

Page 277 of 1250Next

Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .

Class IIModerate

FDAJun 29, 2022Nationwide• Glenmark Pharmaceuticals Inc., USA

Desmopressin Acetate Tablets (Glenmark) – Manufacturing Deviation (2022)

CGMP Deviations

Class IIModerate

FDAJun 29, 2022IN, TX• Glenmark Pharmaceuticals Inc., USA

Telmisartan Hydrochlorothiazide Tablets (Glenmark) – Packaging Issue (2022)

Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .

Class IIModerate

FDAJun 29, 2022Nationwide• Glenmark Pharmaceuticals Inc., USA

Aspirin Dipyridamole Capsules (Glenmark) – Capsule Breakage (2022)

Failed Tablet/Capsule Specification : Capsule breakage

Class IIILow

FDAJun 29, 2022Nationwide• Glenmark Pharmaceuticals Inc., USA

HyVee Oven Baked Beans (Hy-Vee) – potassium sorbate excess (2022)

Baked bean product contains excessive amount of potassium sorbate

Class IIILow

FDAJun 28, 2022IL, IN, IA +6 more• Hy-Vee, Inc. dba Hy-Vee Fresh Commissary

HAMILTON-C6 Intensive Care Ventilator (Hamilton Medical) – Status Board Water Risk (2022)

Ventilator status indicator board can become loose, which could lead to water ingress (disinfectants) that may lead to technical fault alarms. Multiple technical faults in a short time may force ventilators into Safety Ventilation (blower runs constantly) or Ambient Sate (inspiratory channel/expiratory valves opened; patient breaths room air unassisted) with Panel connection lost message displayed

FDAJun 27, 2022Nationwide• Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland

Nifedipine WSP Ointment 0.2% (Valor Compounding) – Potency Issue (2022)

Subpotent and Superpotent Drug

Class IHigh

FDAJun 27, 2022CA• Valor Compounding Pharmacy, Inc DBA Valor Compounding Pharmacy

Divalproex Sodium Tablets 500mg (Sun Pharmaceutical) – Dissolution Failure (2022)

Failed Dissolution Specifications: Failure occurred during routine stability testing of dissolution test.

Class IIModerate

FDAJun 27, 2022Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Za'atar Seasoning (Fuchs) – Salmonella contamination (2022)

Salmonella

The product may be potentially positive for Salmonella due to one of the sub-ingredients (oregano) testing positive for Salmonella.

Class IHigh

FDAJun 27, 2022PA• Fuchs North America, Inc.

2022 AIRSTREAM POTTERY BARN (AIRSTREAM) – Axle Bearing Washer Issue (2022)

Airstream, Inc. (Airstream) is recalling certain 2022 Caravel, Flying Cloud, Globetrotter, International and Pottery Barn travel trailers. The 42mm cartridge bearing washer within the hub assembly may crack, causing the hub to separate from the axle wheel end.

NHTSAJun 24, 2022Nationwide• AIRSTREAM

Daytrana Patch (Noven) – Delivery System Defect (2022)

Defective Delivery System: Customer complaints received for ripping patches and tight release/adhesive transfer.

Class IIModerate

FDAJun 24, 2022Nationwide• Noven Pharmaceuticals Inc