Archive
491 recalls were announced in October 2023.
Of the 491 recalls this month scored against our rubric, 4% are Critical, 28% are Severe.
Which agencies issued them
Vitality Works is recalling 1,025 bottles of fenugreek capsules due to contamination with pieces of a pen. Consumers should stop using the product immediately.
SLR Food Distribution recalled dried longans distributed in seven states because they contain undeclared sulfites. Consumers with sulfite sensitivity may experience adverse reactions.
Vitality Works, Inc. is recalling its 100 vegetarian Fenugreek Capsules due to contamination with pieces of a pen. The affected lot (2023-06871) was distributed to 284 retail locations across the United States.
Cerebelly Inc. has recalled Strawberry Beet flavor Smart Bars (5-pack and 7-pack) due to visible surface mold. Approximately 154,554 selling cartons were distributed across all U.S. states and territories.
Cerebelly Inc is recalling Apple Kale Smart Bars due to visible surface mold contamination. The recall affects all 5-pack and 7-pack sizes distributed nationwide.
Vitality Works is recalling 1,025 bottles of Fenugreek Capsules due to contamination with pieces of a pen. Consumers should stop using the product and return it to the retailer.
J&T Health and Wellness LLC recalls the ProSun Luxura Vegaz Model 52X ultraviolet tanning device due to a potential safety circuit defect. A communication isolator may cause a disturbance that compromises the safety circuit.
Covidien LP is recalling Palindrome Chronic Catheter Kit devices where some catheters labeled as 23 cm implant length actually contain 28 cm devices. The mislabeling could affect proper catheter placement.
3M is recalling 79,500 Attest Super Rapid Readout Biological Indicators because the cap may melt, deform, or crack during steam sterilization cycles, potentially compromising sterilization validation.
Vitality Works is recalling 1,025 bottles of 100-count fenugreek capsules (600mg) due to contamination with pen pieces. The affected lot is 2023-06871, expiring July 2028.
Vitality Works recalls 1,025 bottles of fenugreek capsules containing pieces of a pen. The product was distributed to 284 retail stores across the United States.
Vitality Works recalls 1,025 bottles of fenugreek capsules due to foreign material contamination. The capsules may contain pen pieces and should not be consumed.
Wolf, Henke Sass is recalling Henke-Ject-2 single-use sterile syringes due to potential damage to the sterile barrier that could compromise product sterility. Approximately 216,000 units are affected across the US and Canada.
Vitality Works, Inc. is recalling 1,025 bottles of 100 Vegetarian Fenugreek Capsules due to contamination with pieces of a pen. The affected product was distributed to 284 retail stores across the United States.
Vitality Works, Inc. is recalling 1,025 bottles of 100 vegetarian Fenugreek Capsules 90 count due to contamination with pieces of a pen. No illnesses have been reported.
A batch of NEURACEQ (florbetaben F-18), a radioactive diagnostic drug, was recalled by Sofie after failing sterility assurance testing. The affected batch was distributed to one facility in Virginia.
BD Pyxis MedBank MedPass Software may continue displaying dispensed medication doses as available, risking duplicate medication administration to patients.
Vitality Works is recalling 100 vegetarian Fenugreek Capsules due to contamination with pieces of a writing pen. The recall affects 1,025 bottles distributed to 284 retail locations in the United States.
Vitality Works is recalling 1,025 bottles of fenugreek capsules due to contamination with pen pieces. No illnesses have been reported.
Vitality Works is recalling 1,025 bottles of 100 vegetarian Fenugreek Capsules (600mg) due to pen fragments discovered in some units. No illnesses have been reported.
Vitality Works, Inc is recalling 1,025 bottles of 100 vegetarian Fenugreek Capsules (600mg) due to contamination with pen pieces. The product was distributed to 284 retail stores across the United States.
Vitality Works Inc. is recalling 1,025 bottles of 100 vegetarian Fenugreek Capsules due to contamination with pieces of a pen. Consumers should stop using the product and return or discard it.
IO Inspired Organics Organic Raw Walnuts recalled due to undeclared cashews. The product was distributed in six U.S. states; consumers with tree nut allergies should not consume.
Ambu Inc. is recalling the aView 2 Advance Monitor because multiple impacts can cause the device to short-circuit and potentially combust the lithium-ion battery, resulting in smoke and flames.
Vitality Works is recalling 1,025 bottles of Fenugreek Capsules due to contamination with pen pieces. The affected lot was distributed to retail customers across the United States.
Vitality Works is recalling approximately 1,025 bottles of Fenugreek Capsules due to the presence of pen pieces found in the product. The foreign material poses a potential choking hazard.
Vitality Works is recalling Fenugreek Capsule supplements due to contamination with pen pieces. Affected products were distributed to 284 retail locations across the United States.
Vitality Works is recalling fenugreek capsule bottles due to contamination from pen fragments. The affected lot is 2023-06871, distributed to 284 stores across the United States.
Vitality Works is recalling 1,025 bottles of Fenugreek capsules due to contamination with pieces of a pen. The affected lot was distributed to retail locations across the United States.
Vitality Works, Inc. is recalling 1,025 bottles of Fenugreek Capsules because pen pieces were found in the product. Consumers should stop use and contact the manufacturer for refund instructions.
Vitality Works is recalling 1,025 bottles of its 100-count vegetarian Fenugreek Capsules due to the presence of pen pieces in some units. No illnesses have been reported.
Vitality Works is recalling 1,025 bottles of 100-count Fenugreek Capsules (600mg) due to contamination with pieces of a pen. The recall affects 284 retail locations across the United States.
Vitality Works is recalling 100 vegetarian Fenugreek Capsules due to the presence of pen fragments. The affected bottles were distributed to retail customers in the United States.
Vitality Works is recalling 1,025 bottles of 100 vegetarian Fenugreek Capsules due to contamination with pieces of a writing pen. The product was distributed to 55 retail customers across 284 stores in the United States.
Vitality Works is recalling its 100 vegetarian Fenugreek Capsules due to contamination with pen pieces. The product (lot 2023-06871) was distributed to 55 retail customers across 284 stores in the United States.
Vitality Works is recalling 1,025 bottles of 100-count Fenugreek Capsules (600mg) due to contamination with pen pieces. The affected lot is 2023-06871, distributed to stores across the United States.
Vitality Works is recalling fenugreek supplement capsules (Lot 2023-06871) due to contamination with pen fragments. About 1,025 bottles were distributed to 284 retail store locations across the United States.
Regal Foods is recalling 660 pounds of herbs and garlic products distributed to GA, MD, PA, and KY after rodent feces were found in oregano samples. Consumers should dispose of affected products marked with code 8400.
Vitality Works recalls 1,025 bottles of fenugreek capsules due to contamination with pen pieces. The product poses a potential choking hazard. No illnesses have been reported.
Vitality Works is recalling 1,025 bottles of Fenugreek Capsules (Lot 2023-06871) due to the presence of pen fragments. Consumers who have purchased this product should stop using it immediately.
Vitality Works is recalling 100 vegetarian Fenugreek Capsules (600mg) because bottles may contain pieces of a pen, posing a choking hazard.
Cerebelly Inc is recalling Cerebelly Smart Bar in Blueberry Banana flavor due to visible surface mold. The recall affects 154,554 cases distributed to all 50 U.S. states and territories.
Regal Foods, Inc is recalling REGAL PASTA HERB 4oz packages due to rodent feces found in oregano samples. The product was distributed to GA, MD, PA, and KY.
Vitality Works is recalling fenugreek capsule bottles due to the presence of pen pieces in the product. The contamination affects 1,025 bottles distributed to retail customers across the United States.
Vitality Works is recalling Fenugreek Capsules (90-count, 600mg) due to contamination with pen fragments. The recalled product was distributed to 55 retail customers across the United States.
Vitality Works recalls 100 vegetarian Fenugreek Capsules due to foreign material contamination. Approximately 1,025 bottles containing pen pieces have been distributed to 284 retail locations nationwide.
Vitality Works is recalling 1,025 bottles of 100 vegetarian Fenugreek Capsules due to contamination with pieces of a pen. Consumers should stop using the product immediately.
Vitality Works, Inc is recalling 1,025 bottles of Fenugreek Capsules (90 count, 600mg) because they may contain pieces of a pen. Consumers should stop using the product and contact the manufacturer for a refund.
Regal Foods, Inc. is recalling 674 lbs of Regal Italian Seasoning because rodent feces was found in oregano samples. The product was distributed in Georgia, Maryland, Pennsylvania, and Kentucky.
Vitality Works Inc is recalling 100 Vegetarian Fenugreek Capsules due to pen fragments found in the product. The recall affects approximately 1,025 bottles distributed across 284 retail stores in the United States.
Vitality Works is recalling Fenugreek Capsules due to contamination with pen fragments discovered during manufacturing. The recall affects approximately 1,025 bottles distributed across U.S. retailers.
Vitality Works is recalling 1,025 bottles of Fenugreek Capsules due to contamination with pieces of a pen (writing utensil). The affected product was distributed to 284 retail stores across the United States.
Vitality Works is recalling 1,025 bottles of Fenugreek Capsules (Lot 2023-06871) because they contain pen fragments. Consumers who purchased this lot should not use the product.
Mini Cigars from Ice Cream House are recalled due to potential Listeria monocytogenes contamination. The products were distributed in Ohio, New Jersey, and New York.
Regal Foods is recalling Regal Herbs De Provence seasoning after rodent feces were found in oregano samples. The product was distributed in Georgia, Maryland, Pennsylvania, and Kentucky.
Vitality Works is recalling 1,025 bottles of Fenugreek Capsules (Lot 2023-06871) due to foreign pen pieces found in the product. The recall affects 284 retail stores across the United States.
Vitality Works is recalling 1,025 bottles of 100 Vegetarian Fenugreek Capsules (600mg, 90-count) due to the presence of pen fragments discovered in the product. Affected lot 2023-06871 (expires 07/2028) was distributed to 284 stores nationwide.
Vitality Works, Inc is recalling 1,025 bottles of 100 Vegetarian Fenugreek Capsules (600mg) due to the presence of pen fragments. No illnesses or injuries have been reported.
Regal Foods is recalling Regal Fajita Seasoning distributed in Georgia, Maryland, Pennsylvania, and Kentucky because rodent feces was found in oregano samples.
Regal Foods, Inc. is recalling Regal Blackening Season seasoning due to rodent feces found in oregano samples. The product was distributed to Georgia, Maryland, Pennsylvania, and Kentucky.
Vitality Works is recalling 1,025 bottles of 100 vegetarian Fenugreek Capsules (600mg) due to the presence of pen pieces. No illnesses have been reported.
Vitality Works is recalling 1,025 bottles of 100 vegetarian Fenugreek Capsules due to contamination with pen pieces. The affected capsules were distributed to 284 retail locations across the United States.
Ice Cream House is recalling Triangle Up Strawberry Mango Vanilla ice cream sold in Ohio, New Jersey, and New York due to potential Listeria monocytogenes contamination. No illnesses have been reported.
The Aquilex Fluid Control System (Models AQL-100PBS, AQL-100P) display may freeze at maximum volume (30,000 ml) during long procedures, causing inaccurate fluid monitoring and potential fluid overload.
Dental planning software exoplan 3.1 contains a filtering error that may display all surgical guide options instead of only supported ones, potentially causing patient injury.
Stryker Corporation is recalling 96 units of the expired Cinchlock SS Knotless Anchor Inserter (Part Number CAT02462, Lot 19175AE2) distributed nationwide. Expired surgical devices may not perform reliably during use.
Inmar Supply Chain Solutions recalled various medical devices nationwide due to potential rodent exposure and temperature excursions. Affected products include bandages, tampons, condoms, blood glucose monitors, adult diapers, COVID-19 test kits, and pregnancy tests.
Waldemar Link is recalling 8 units of the MobileLink Acetabular Cup System due to labeling with an incorrect offset specification. The mislabeling could affect proper surgical placement of this orthopedic implant.
3M is recalling 77,280 Attest biological indicators due to caps that may melt, deform, or crack during steam sterilization cycles, potentially compromising process validation.
3M is recalling specific lots of Attest biological indicators used in steam sterilization monitoring. Certain lots have caps that may melt, deform, or crack at sterilization temperatures of 132°C and 135°C, potentially compromising sterilization process verification.
Fresenius Kabi USA has recalled Ivenix Infusion System Large Volume Pump software versions 5.0.0 and 5.0.1 due to startup time delays that may exceed 6 minutes at flow rates between 50-200 ml/hr.
3M is recalling 172,464 units of Attest biological indicators used to validate steam sterilization because caps may melt, deform, or crack during sterilization at 132°C and 135°C.
RB Health (US) is recalling Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%) due to an incorrect label on the back of the packaging. The recall affects 36,426 individual units distributed nationwide.
Tolmar, Inc. is recalling Eligard (leuprolide acetate) 7.5 mg monthly injectable suspension nationwide because the constituted product contains higher than expected levels of the active ingredient. The affected lot is 13635A1 with expiration date July 31, 2024.
Moreflavor, Inc. recalled 44 one-pound bags of CellarScience ascorbic acid (batch 56559) due to labeling error: bags labeled as ascorbic acid contain sodium percarbonate.
Vitality Works, Inc. is recalling its 100 Vegetarian Fenugreek Capsules due to contamination with pen pieces. The recall affects 1,025 bottles distributed to 284 retail stores across the United States.
Vitality Works is recalling 1,025 bottles of Fenugreek Capsules (Lot 2023-06871) due to contamination with pen pieces. The product was distributed to 284 retail stores across the United States.
Ozona Organics LLC is recalling Ozona Organics and Go Healthy Liquid Probiotics nationwide due to high water activity in the formula that could allow microbial growth. No illnesses have been reported.
Vitality Works, Inc. is recalling 100 vegetarian fenugreek capsules (600mg) because some bottles contain pen fragments. Approximately 1,025 bottles were distributed to retail stores across the United States.
Pharma-Natural Inc. is recalling Pharma Natural Biotin 5000 mcg dietary supplement (Lot PN10686, Exp. Date 01/24) distributed in Puerto Rico because FDA testing found the biotin content was below the detection limit.
Baxter Healthcare issued an urgent correction for the Epiphany Cardio Server E3 ECG Management System because the caliper tool may become non-responsive, temporarily preventing its use. Affects 89 units distributed across the US, Canada, and Bermuda.
Volvo Bus is recalling 2023 9700 vehicles because power cable fasteners may not be tightened securely, which can cause overheating and increase the risk of a fire.
Volvo Bus is recalling 2023 9700 buses because emergency window exits may lack required identification and operating instruction labels.
Daimler Trucks is recalling certain 2019-2024 Thomas Built SAF-T-LINER school buses because the emergency exit door fasteners may loosen and detach, potentially allowing the door to open unexpectedly.
Zero Motorcycles is recalling accessory chain kits because incorrect installation instructions may cause the motor shaft magnet to dislocate, increasing crash risk.
Certain 2019-2024 Thomas Built SAF-T-LINER C2 transit buses are being recalled because fasteners for the emergency exit door may loosen and detach, causing the door to open unexpectedly and increasing risk of injury.
Mando America Corporation is recalling ABS modules that may leak brake fluid and cause electrical shorts, leading to engine compartment fires.
Harley-Davidson is recalling 2023 X350RA motorcycles because a fuel sensor may leak fuel, increasing the risk of fire.
REV Recreation Group is recalling certain 2024 Holiday Rambler Invicta motorhomes. The exterior griddle may be stowed while still connected to the LP gas line, creating a fire risk.
Continental is recalling specific CrossContact LX25 tires because metal fragments in the rubber may cause sudden air loss and increase crash risk.
Mercedes-Benz is recalling 2022 A 220, GLA 250, and AMG GLA35 vehicles because incorrectly adjusted headlights may reduce visibility and increase crash risk.
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