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Bausch & Lomb Inc

Bausch & Lomb Inc Recalls

All product recalls associated with Bausch & Lomb Inc.

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Recall Summary

Total Recalls

1000

Past Year

295

Class I (Serious)

116

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 3741–3760 of 4465 recalls

Bausch & Lomb Inc: Bausch & Lomb ReNu Multi-Purpose Solution, 12 fl.oz. (355...

During routine testing the product failed to meet shelf life specifications.

FDAAug 17, 2009Nationwide• Bausch & Lomb Inc

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: BrainLab Radiotherapy Treatment Planning Software; Cata...

Failure to conduct important safety checks when using the BrainLab radiotherapy treatment planning software in combination with BrainLab conical collimators could result in unintended radiation outside the conical shaped field, which may lead to serious injury of the patient.

FDAAug 12, 2009Nationwide• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Davol, Inc., Sub. C. R. Bard, Inc.: BARD Simpulse" SOLO System with Soft Splash Shield Tip P...

Product sterility may be compromised due to lack of package integrity.

1...186 187188189 190...224

Page 188 of 224Next

FDA

Jul 30, 2009

Nationwide

• Davol, Inc., Sub. C. R. Bard, Inc.

BabyBjörn Babysitter Balance Bouncer Chairs – laceration risk (2009)

Laceration Risk

The recall involves the BabyBjörn's Babysitter Balance and Babysitter Balance Air bouncers. These bouncing chairs for babies have a red safety latch on the height adjustment mechanism and a plastic footrest with the BabyBjörn® logo. Recalled models and colors are: BabyBjörn® Babysitter Balance: Black/Red; Model #009064US Black/Silver; Model #009065US Dark Blue/Blue; Model #009066US Brown/Beige; Model #009069US BabyBjörn® Babysitter Balance Air: White; Model 009001US

CPSCJul 28, 2009Nationwide• BabyBjörn AB, of Sweden

Abbott Laboratories, Inc: ARCHITECT i2000 System and ARCHITECT i2000 SR wash buffer...

Under certain conditions, the product's wash buffer containing sodium azide can come in contact with the wash zone mechanism ground cables on either of the two wash zones. The copper in the ground strap may corrode and form an unstable chemical substance (metal azide) that may be sensitive to direct pressure and impact.

FDAJul 17, 2009Nationwide• Abbott Laboratories, Inc

Abbott Laboratories: CELL-DYN Emerald Hematology Analyzer, model number 09H39-...

Software bug. The CELL-DYN Emerald WBC L1 flag is configured incorrectly. The flag is not generated according to system requirements.

FDAJul 16, 2009Nationwide• Abbott Laboratories

Bio-Rad Laboratories Inc: BIO-RAD 425-2020 Autoimmune EIA Anti-Cardiolipin IgM, 96 ...

The firm received customer complaints of microbial contamination in Positive Controls in its Anti-Cardiolipin IgM Test Kit Lot CL-863.

FDAJul 14, 2009Nationwide• Bio-Rad Laboratories Inc

Leonhard Lang Gmbh Archenweg 56 Innsbruck Austria: S&W Electrodes for Defibrillation, 10 Defibrillation Elec...

A potential risk was identified associated with the connectors of the defibrillation electrodes DF20. It was found that some of the connectors do not slip easily into the sockets of the defibrillator or an extension cord of the defibrillator. In such cases increased force or some wiggling is required to insert the connector fully. A potential risk for patients exist, if (a) such a connector (b)

FDAJul 10, 2009FL• Leonhard Lang Gmbh Archenweg 56 Innsbruck Austria

Leonhard Lang Gmbh Archenweg 56 Innsbruck Austria: SKINTACT Electrodes for Defibrillation, 10X REF DF20, Rx ...

FDAJul 10, 2009FL• Leonhard Lang Gmbh Archenweg 56 Innsbruck Austria

Abbott Laboratories Inc.: Clinical Chemistry Total Bilirubin, 6L45-20 and 6L45-40. ...

Abbott Laboratories has issued a recall on the Clinical Chemistry Total Bilirubin due to an under-recovery on one clinical neonatal specimen resulting in a value less than the assay linear limit.

FDAJul 9, 2009PR• Abbott Laboratories Inc.

Kidde Smoke Alarms (Walter Kidde) - Fire Warning Failure (2009)

Fire/Burn Risk

This recall involves Kidde dual sensor smoke alarms model PI2000. The alarms can be identified by two buttons, "HUSH" and "PUSH AND HOLD TO TEST WEEKLY," which are located on the front/center of the alarm. The model number and date code are on the back of the smoke alarm. Only date codes 2008 Aug.01 through 2009 May 04 are included in this recall.

CPSCJul 9, 2009Nationwide• Walter Kidde Portable Equipment Inc., of Mebane, N.C.

Bausch & Lomb Inc: Bausch & Lomb, Boston Conditioning Solution, Original For...

The product failed to meet one of the shelf life specifications at the end of the expiry period.

FDAJun 30, 2009Nationwide• Bausch & Lomb Inc

B. Braun Interventional Systems: Celsite Access Port Model ST305P. The Celsite Access Por...

B. Braun Interventional Systems was notified by B. Braun Medical France, the manufacturer of the Celsite Access port that they had received 11 reports of polyurethane (type P) catheter disconnections. B. Braun Medical France has decided to recall all Celsite ports supplied with the affected catheter lot. To date, B. Braun Interventional Systems (US) has not received any reports of catheter dis

FDAJun 22, 2009Nationwide• B. Braun Interventional Systems

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: POWERSAIL Coronary Dilatation Catheter: 3.25x18mm (US) Pa...

Distal shaft of the POWERSAIL coronary Dilatation Catheters exhibits damage that may result in a leak of contrast material and functional failures.

FDAJun 17, 2009Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Bio-Rad Laboratories Inc: Bio-Rad VARIANT II Hemoglobin A1c Program Recorder Pack w...

Calibration Failure-- due to high intercept values, the device fails calibration and users are unable to run samples.

FDAJun 15, 2009Nationwide• Bio-Rad Laboratories Inc

Abbott Diabetes Care, Inc.: FreeStyle Lite Blood Glucose Test Strips, CSP, 50's US, C...

Low results: Freestyle Lite Blood Glucose Test strip may generate low blood glucose readings when tested with the control solution from lot 0822524 with Freestyle Freedom Lite and Freestyle Lite Blood Glucose Meters.

FDAJun 10, 2009AL, AZ, CA +14 more• Abbott Diabetes Care, Inc.

Abbott Laboratories: CELL-DYNE 1700CS (Closed Sampler), list numbers 03H57-01,...

Use of Syringe LN 04H36-01 with the Die-cast syringe drive may result in leakage, leading to delay in reporting patient results.

FDAJun 8, 2009Nationwide• Abbott Laboratories

Abbott Laboratories: CELL-DYN 1800, list numbers 07H77-01, 07H77-03, manufactu...

Use of Syringe LN 04H36-01 with the Die-cast syringe drive may result in leakage, leading to delay in reporting patient results.

FDAJun 8, 2009Nationwide• Abbott Laboratories

Abbott Laboratories: CELL-DYN 1700, list numbers 03H5301 and 03H53-03, manufa...

Use of Syringe LN 04H36-01 with the Die-cast syringe drive may result in leakage, leading to delay in reporting patient results.

FDAJun 8, 2009Nationwide• Abbott Laboratories

Bee Strollers (Bugaboo) – brake failure (2009)

Bugaboo Bee strollers have item code 580210 on a label on the back of the seat and item code 50100 on a label on the plastic support under the seat. The strollers were sold in blue, dark khaki, pink, red, yellow, and black. "bugaboo® bee" is printed on the left side of the seat.

CPSCJun 2, 2009Nationwide• Bugaboo Design & Sales, B.V., of the Netherlands