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Boothwyn Pharmacy LLC

Boothwyn Pharmacy LLC Recalls

All product recalls associated with Boothwyn Pharmacy LLC.

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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 641–660 of 25000 recalls

Semaglutide Injection (Boothwyn Pharmacy) – Subpotent Drug (2025)

Subpotent Drug

Class IIModerate

FDAJul 9, 2025Nationwide• Boothwyn Pharmacy LLC

Semaglutide Injection (Boothwyn Pharmacy) – Potency Issue (2025)

Subpotent Drug

Class IIModerate

FDAJul 9, 2025Nationwide• Boothwyn Pharmacy LLC

Ambu SPUR II (Ambu Inc.) – Manometer Port Blockage (2025)

Potential for the manometer port being blocked rendering the manometer non-functional.

Low

FDAJul 9, 2025

1...31 323334 35...1250

Page 33 of 1250Next

Nationwide

• Ambu Inc.

Fluorescein 2% Ophth (Boothwyn Pharmacy) – Subpotent Drug (2025)

Subpotent Drug

Class IIILow

FDAJul 9, 2025Nationwide• Boothwyn Pharmacy LLC

BD Trucount Controls (BD Bio Sciences) – Incorrect SD Values (2025)

Control kits contain incorrect standard deviation (SD) values for the low and high control beads which compromises the accurate calculation of bead counts.

Low

FDAJul 8, 2025Nationwide• Becton, Dickinson and Company, BD Bio Sciences

Reading Rail Gear Trucks HD (Reading) – Weld Crack Risk (2025)

Reading Truck Body, LLC (Reading) is recalling certain 2021 Rail Gear HD trucks. Welds may crack and fail, allowing the front rail gear to shift and contact the road.

High

NHTSAJul 7, 2025Nationwide• READING TRUCK EQUIPMENT

Can-Am Canyon (Can-Am) – Drive Belt Support Problem (2025)

Bombardier Recreational Products, Inc. (BRP) is recalling certain 2025 Can-Am Canyon motorcycles. On these motorcycles, the drive belt lower idler support will fail and possibly cause a belt failure.

High

NHTSAJul 3, 2025Nationwide• CAN-AM

t:slim X2 Insulin Pump (Tandem) – App Pairing Issue (2025)

an app defect that occurs when the phone is set to a right-to-left language, which causes app-pump pairing issues and graphical defects, which can potentially lead to incorrect therapy decisions and subsequent hypoglycemia or hyperglycemia.

High

FDAJul 3, 2025Nationwide• Tandem Diabetes Care, Inc.

Evergreen Farm Grape Juice – Sanitation Concern (2025)

Lack of pasteurization and sanitation records

Class IIModerate

FDAJul 3, 2025NJ, NY, PA• Evergreen Orchard Farm, LLC

Evergreen Farm Korean Pear Juice – Sanitation Concern (2025)

Lack of pasteurization and sanitation records

Class IIModerate

FDAJul 3, 2025NJ, NY, PA• Evergreen Orchard Farm, LLC

Evergreen Farm Jujube Juice – Sanitation Concern (2025)

Lack of pasteurization and sanitation records

Class IIModerate

FDAJul 3, 2025NJ, NY, PA• Evergreen Orchard Farm, LLC

GE OEC 9800 (GE Medical Systems) – Regulatory Non-Conformance (2025)

GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.

Moderate

FDAJul 2, 2025Nationwide• GE Medical Systems, LLC

Sparrow Ascent Patient Controller (Spark Biomedical) – Cable Disconnect (2025)

Due to manufacturing issue, neurostimulator device may experience "cable disconnect" error message and interruption to stimulation output.

Moderate

FDAJul 2, 2025Nationwide• Spark Biomedical Inc

Smoked Gouda (Boar's Head) – Mislabeling (2025)

Mislabeling

Class IIILow

FDAJul 2, 2025FL• Alpine Slicing and Cheese Conversion Company

Amlodipine Benazepril Capsules (Lupin) – Incorrect Expiration (2025)

Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 instead of Jan.2027

Class IIModerate

FDAJul 2, 2025Nationwide• Lupin Pharmaceuticals Inc.

GE OEC 9900 Elite C-arm Systems (GE Medical Systems) – Non-Conformance (2025)

Moderate

FDAJul 2, 2025Nationwide• GE Medical Systems, LLC

Junctional Emergency Treatment Tool (North American Rescue) – Manufacturing Defect (2025)

Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device and device performance during use.

Low

FDAJul 1, 2025Nationwide• North American Rescue LLC.

Peripheral Parenteral Nutrition (CAPS) – Processing Controls (2025)

Lack of Processing Controls; prescriptions were compounded in an ISO-5 area where it was identified that a daily cleaning step was not sufficiently documented.

Class IIModerate

FDAJul 1, 2025CA• Central Admixture Pharmacy Services, Inc (CAPS) Los Angeles

Ingenia 3.0T CX (Philips) – Gradient Coil Failure (2025)

Fire/Burn Risk

The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.

High

FDAJun 30, 2025Nationwide• Philips North America

MR 7700 (Philips) – Gradient Coil Failure (2025)

Fire/Burn Risk

The potential for component failures in the Gradient Coil of the affected MR systems may act as a heat source with a potential to produce smoke and/or fire.

High

FDAJun 30, 2025Nationwide• Philips North America