replacement available Recalls

280 recalls tagged with “replacement available”.

Health & Personal Care
HIGH
FDA DRUG

ACME UNITED Instant Hand Sanitizing Wipes Recalled for CGMP Deviations (2026)

ACME UNITED recalled instant hand sanitizing wipes nationwide after FDA flagged CGMP deviations. The product, labeled for Children’s Healthcare of Atlanta and manufactured in the USA, contains benzalkonium chloride 0.13% and is sold 1,000 wipes per case under NDC 0924-7130-00. Consumers and healthcare providers should stop using this product immediately and contact ACME UNITED CORPORATION for next

ACME UNITED
CGMP Deviations
Read more
Health & Personal Care
HIGH
FDA DRUG

Acme United MED NAP BZK Antiseptic Towelettes Recalled in 2026 (100-Count)

Acme United Corporation recalled Med Nap BZK Antiseptic Towelettes, 100-count, distributed nationwide. The FDA-listed CGMP deviations raise concerns about manufacturing quality and product safety. Consumers and healthcare providers should stop using the product and follow the recall letter for guidance.

Acme United Corporation
CGMP Deviations
Read more
Health & Personal Care
HIGH
FDA DRUG

ACME UNITED Antimicrobial Hand Wipes Recall 2026 for CGMP Deviations

ACME UNITED recalled antimicrobial hand wipes manufactured for Custom Packaging Co., Inc. and distributed nationwide in the United States. The recall cites CGMP deviations in manufacturing. Consumers and healthcare providers should stop using this product immediately and contact ACME UNITED for guidance.

ACME UNITED
CGMP Deviations
Read more
Health & Personal Care
HIGH
FDA DRUG

ACME United's First Aid Only BZK Towelettes Recall 2026: CGMP Deviations Prompt Nationwide Action

ACME United Corporation recalled First Aid Only BZK Antiseptic Towelettes nationwide after CGMP deviations were identified in manufacturing. The products carry NDC 0924-7116-03 and come in 50-wipe packages. Consumers should stop using the product and contact the company for guidance. A recall notice will be mailed to affected customers.

First Aid Only
CGMP Deviations
Read more
Health & Personal Care
HIGH
FDA DRUG

ACME United BZK Antiseptic Towelettes Recall for CGMP Deviations (2026)

ACME United Corporation recalled BZK Antiseptic Towelettes sold for Food Service Resources nationwide after CGMP deviations were found. The recall is Class II and high risk. Consumers and healthcare providers should stop using this product immediately and follow recall guidance.

ACME United
CGMP Deviations
Read more
Health & Personal Care
HIGH
FDA DRUG

ACME United Recalls Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes (2026)

ACME United recalled Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes sold nationwide on Jan. 20, 2026. The recall cites CGMP deviations in manufacturing. Consumers and healthcare providers should stop using the product immediately and contact ACME United or their healthcare provider for guidance.

ACME United
CGMP Deviations
Read more
Health & Personal Care
HIGH
FDA DEVICE

Siemens Healthcare Diagnostics Recalls 4,885 Atellica CH Urine Albumin Tests for False Low Results (

Siemens Healthcare Diagnostics recalled 4,885 Atellica CH Urine Albumin tests in 2026 after detecting falsely depressed results. The manufacturer notes that any urine albumin concentration above 40.0 mg/dL may report values from 6.2 to 40.0 mg/dL. Stop using the device immediately and follow the recall instructions.

Siemens Healthcare Diagnostics
Falsely depressed
Read more
Health & Personal Care
HIGH
FDA DEVICE

Roche Cobas Pro 1,261-Unit Recall Over Spline-Calibration Error (2026)

Roche Diagnostics issued a nationwide recall of 1,261 Cobas Pro systems with cobas c 503 units in the United States. A software defect can cause erroneous, non-monotonic calibrations for spline-type assays. Labs should stop using the devices immediately and follow the manufacturer's recall instructions.

Roche Diagnostics Operations
Software defect,
Read more
Health & Personal Care
HIGH
FDA DRUG

Med-Nap Cleansing Towelettes Recall 2026 for CGMP Deviations

Med-Nap Cleansing Towelettes, manufactured by Acme United Corporation, were recalled nationwide on January 20, 2026. The recall cites CGMP deviations in manufacturing for benzalkonium chloride 0.13% towelettes. Consumers and healthcare providers should stop using the product immediately and contact Acme United for guidance.

Med-Nap Cleansing Towelettes
CGMP Deviations
Read more
Food & Beverages
HIGH
FDA FOOD

Frederik's by Meijer Focaccia Bread Recalled for Metal Fragments (2026)

Frederik's by Meijer Slow-Roasted Tomato & Parmesan Focaccia Bread recalled after metal fragments were found in 23,459 cases. The recalls spans Frederik's by Meijer, Fresh & Simple, HT Traders and Trader Joe's focaccia products. The metal fragments were traced to roasted tomatoes from an ingredient supplier. Stop using the product and contact the supplier for refunds or replacements.

Bakkavor
Metal fragments
Read more
Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare Centricity Universal Viewer ZFP Recall 250 Units Worldwide in 2026

GE Healthcare recalled 250 Centricity Universal Viewer Zero Footprint Client units distributed worldwide after finding a risk that patient information may not match displayed images in certain workflows. The issue affects ZFP v6.0 SP11.6, SP11.6.0.1 and SP11.6.1 when Patient Timeline is installed. Hospitals should stop using affected units and await instructions from GE Healthcare.

GE Healthcare
Under certain
Read more
Food & Beverages
HIGH
FDA FOOD

Bader Enterprises Recalls Premium Food Jordan Almonds in 2.0 oz & 3.5 oz Packaging (2026 Recall)

Bader Enterprises recalls 60 pounds of Premium Food Jordan Almonds sold in New Jersey and New York. The product contains undeclared wheat and blue color additives. Consumers who purchased the product should not consume it. Contact Bader Enterprises for refund or replacement information via two or more notification methods.

Bader Enterprises
Contains undeclared
Read more
Health & Personal Care
HIGH
FDA DEVICE

Aesculap MINOP TROCAR 150MM Recall for 126 Units in 2026

Aesculap recalls 126 MINOP TROCAR 150MM devices distributed nationwide to U.S. hospitals and clinics after regulators flagged a shaft length issue. The shaft may be longer than specified, potentially harming tissue during procedures. Healthcare facilities should stop using the devices and follow manufacturer recall instructions immediately.

Aesculap
There is
Read more
Food & Beverages
HIGH
FDA FOOD

Sevillo Fine Foods Recalls 520 Units of Slow Roasted Diced Tomatoes Over Metal Fragments (2026)

Sevillo Fine Foods recalled 520 units of Slow Roasted Diced Tomatoes distributed to California and North Carolina after the product may contain metal fragments. The product is frozen and packaged in bulk with a plastic liner inside a cardboard box. Consumers should not eat the product and should contact Sevillo Fine Foods for refund or replacement via email.

Sevillo Fine Foods
Product may
Read more
Food & Beverages
HIGH
FDA FOOD

Rose and Shore Recalls 5,067.1 Cases of 14" Margarita Thin Crust Pizza for Metal Fragments (2026)

Rose and Shore recalled 5,067.1 cases of 14" Margarita Thin Crust Pizza sold at a single regional chain in California, Oregon, Arizona, Idaho and Texas. A potential foreign object has been found in tomatoes used in the product. Consumers should not eat this pizza and should contact Rose and Shore for refund or replacement by email.

Rose and Shore
potential foreign
Read more
Recalled Loam Pedal Gen 2 aluminum alloy bicycle pedal
MEDIUM
CPSC

PNW Components Recalls Bicycle Pedals Over Crash Hazard

PNW Components recalled its Loam Pedal Gen 2 on January 9, 2026, after reports of axle cracks. The defect can cause pedals to detach, posing a fall risk. Customers should stop using the pedals immediately and seek replacements.

PNW Components
The pedal
Read more